Canonical Allele Identifier: CA377360897
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs1675797746

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275172T>C , CM000672.2:g.80275172T>C GRCh38
NC_000010.10:g.82034928T>C , CM000672.1:g.82034928T>C GRCh37
NC_000010.9:g.82024908T>C NCBI36
NG_008083.1:g.19507A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.796A>G MANE Select ENSP00000361287.3:p.Ile266Val
ENST00000372213.7:c.796A>G ENSP00000361287.3:p.Ile266Val
ENST00000480845.1:n.28A>G
ENST00000485270.5:n.308A>G
NM_000429.2:c.796A>G NP_000420.1:p.Ile266Val
XM_005269842.3:c.796A>G XP_005269899.1:p.Ile266Val
XM_005269843.3:c.673A>G XP_005269900.1:p.Ile225Val
NM_000429.3:c.796A>G MANE Select NP_000420.1:p.Ile266Val