Canonical Allele Identifier: CA2722252813
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs2132705988
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280465A>G , CM000672.2:g.80280465A>G GRCh38
NC_000010.10:g.82040221A>G , CM000672.1:g.82040221A>G GRCh37
NC_000010.9:g.82030201A>G NCBI36
NG_008083.1:g.14214T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-149T>C MANE Select ENSP00000361287.3:n.406-149T>C
ENST00000372213.7:c.406-149T>C ENSP00000361287.3:n.406-149T>C
ENST00000455001.1:c.217-149T>C ENSP00000414961.1:n.217-149T>C
NM_000429.2:c.406-149T>C NP_000420.1:n.406-149T>C
XM_005269842.3:c.406-149T>C XP_005269899.1:n.406-149T>C
XM_005269843.3:c.283-149T>C XP_005269900.1:n.283-149T>C
NM_000429.3:c.406-149T>C MANE Select NP_000420.1:n.406-149T>C
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