Canonical Allele Identifier: CA2317700493
Gene: GAMT HGNC NCBI

Linked Data

dbSNP Id: rs1600160780
gnomAD v4: 19-1401486-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401486T>C , CM000681.2:g.1401486T>C GRCh38
NC_000019.9:g.1401485T>C , CM000681.1:g.1401485T>C GRCh37
NC_000019.8:g.1352485T>C NCBI36
NG_009785.1:g.5068A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.-10A>G MANE Select ENSP00000252288.1:n.-10A>G
ENST00000447102.8:c.-10A>G ENSP00000403536.2:n.-10A>G
ENST00000640762.1:c.-10A>G ENSP00000492031.1:n.-10A>G
ENST00000252288.6:c.-10A>G ENSP00000252288.1:n.-10A>G
ENST00000447102.7:c.-10A>G ENSP00000403536.2:n.-10A>G
NM_000156.5:c.-10A>G NP_000147.1:n.-10A>G
NM_138924.2:c.-10A>G NP_620279.1:n.-10A>G
NM_000156.6:c.-10A>G MANE Select NP_000147.1:n.-10A>G
NM_138924.3:c.-10A>G NP_620279.1:n.-10A>G