Canonical Allele Identifier: CA1922574400
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs1841484461
gnomAD v4: 10-80276261-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80276261T>A , CM000672.2:g.80276261T>A GRCh38
NC_000010.10:g.82036017T>A , CM000672.1:g.82036017T>A GRCh37
NC_000010.9:g.82025997T>A NCBI36
NG_008083.1:g.18418A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.768+115A>T MANE Select ENSP00000361287.3:n.768+115A>T
ENST00000372213.7:c.768+115A>T ENSP00000361287.3:n.768+115A>T
NM_000429.2:c.768+115A>T NP_000420.1:n.768+115A>T
XM_005269842.3:c.768+115A>T XP_005269899.1:n.768+115A>T
XM_005269843.3:c.645+115A>T XP_005269900.1:n.645+115A>T
NM_000429.3:c.768+115A>T MANE Select NP_000420.1:n.768+115A>T
Search 100 bp 5'
Search 100 bp 3'