Canonical Allele Identifier: CA3104830607
Community Standard Title: NC_000003.12:g.10141777C=
Gene: VHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.10141777C= , CM000665.2:g.10141777C= GRCh38
NC_000003.11:g.10183461C= , CM000665.1:g.10183461C= GRCh37
NC_000003.10:g.10158461C= NCBI36
NG_008212.3:g.5143C= , LRG_322:g.5143C=

Transcript Alleles

HGVS Amino-acid Change
NM_000551.3:c.-71C= , LRG_322t1:c.-71C= NP_000542.1:n.-71C=
NM_001354723.1:c.-71C= NP_001341652.1:n.-71C=
NM_198156.2:c.-71C= NP_937799.1:n.-71C=
ENST00000256474.2:c.-71C= ENSP00000256474.2:n.-71C=
XM_011534078.1:c.-71C= XP_011532380.1:n.-71C=