Canonical Allele Identifier: CA377362095
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82036248T>C (hg19) chr10:g.80276492T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80276492T>C , CM000672.2:g.80276492T>C GRCh38
NC_000010.10:g.82036248T>C , CM000672.1:g.82036248T>C GRCh37
NC_000010.9:g.82026228T>C NCBI36
NG_008083.1:g.18187A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.652A>G MANE Select ENSP00000361287.3:p.Met218Val
ENST00000372213.7:c.652A>G ENSP00000361287.3:p.Met218Val
NM_000429.2:c.652A>G NP_000420.1:p.Met218Val
XM_005269842.3:c.652A>G XP_005269899.1:p.Met218Val
XM_005269843.3:c.529A>G XP_005269900.1:p.Met177Val
NM_000429.3:c.652A>G MANE Select NP_000420.1:p.Met218Val
Search 100 bp 5'
Search 100 bp 3'