Canonical Allele Identifier: CA432423289
Gene: VHL HGNC NCBI

Linked Data

dbSNP Id: rs1461479062
gnomAD v2: 3-10191508-G-T
gnomAD v4: 3-10149824-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10149824G>T , CM000665.2:g.10149824G>T GRCh38
NC_000003.11:g.10191508G>T , CM000665.1:g.10191508G>T GRCh37
NC_000003.10:g.10166508G>T NCBI36
NG_008212.3:g.13190G>T , LRG_322:g.13190G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696142.1:c.*178G>T ENSP00000512434.1:n.*178G>T
ENST00000696143.1:c.637G>T ENSP00000512435.1:n.637G>T
ENST00000696153.1:c.612G>T ENSP00000512444.1:p.Arg204=
ENST00000256474.3:c.501G>T MANE Select ENSP00000256474.3:p.Arg167=
ENST00000256474.2:c.501G>T ENSP00000256474.2:p.Arg167=
ENST00000345392.2:c.378G>T ENSP00000344757.2:p.Arg126=
ENST00000477538.1:n.637G>T
NM_000551.3:c.501G>T , LRG_322t1:c.501G>T NP_000542.1:p.Arg167=
NM_198156.2:c.378G>T NP_937799.1:p.Arg126=
NM_001354723.1:c.*55G>T NP_001341652.1:n.*55G>T
NM_000551.4:c.501G>T MANE Select NP_000542.1:p.Arg167=
NM_001354723.2:c.*55G>T NP_001341652.1:n.*55G>T
NM_198156.3:c.378G>T NP_937799.1:p.Arg126=