Canonical Allele Identifier: CA2499225407
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1111585
ClinVar RCV Id: RCV001438247
dbSNP Id: rs1479331383
gnomAD v4: 19-1399948-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399948C>A , CM000681.2:g.1399948C>A GRCh38
NC_000019.9:g.1399947C>A , CM000681.1:g.1399947C>A GRCh37
NC_000019.8:g.1350947C>A NCBI36
NG_009785.1:g.6606G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.182-10G>T MANE Select ENSP00000252288.1:n.182-10G>T
ENST00000447102.8:c.182-10G>T ENSP00000403536.2:n.182-10G>T
ENST00000640762.1:c.113-10G>T ENSP00000492031.1:n.113-10G>T
ENST00000252288.6:c.182-10G>T ENSP00000252288.1:n.182-10G>T
ENST00000447102.7:c.182-10G>T ENSP00000403536.2:n.182-10G>T
NM_000156.5:c.182-10G>T NP_000147.1:n.182-10G>T
NM_138924.2:c.182-10G>T NP_620279.1:n.182-10G>T
NM_000156.6:c.182-10G>T MANE Select NP_000147.1:n.182-10G>T
NM_138924.3:c.182-10G>T NP_620279.1:n.182-10G>T
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