Canonical Allele Identifier: CA1266821981
Gene: MAT2A HGNC NCBI

Linked Data

dbSNP Id: rs1573307518
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540649C>T , CM000664.2:g.85540649C>T GRCh38
NC_000002.11:g.85767772C>T , CM000664.1:g.85767772C>T GRCh37
NC_000002.10:g.85621283C>T NCBI36
NG_029183.1:g.6672C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306434.8:c.92-434C>T MANE Select ENSP00000303147.3:n.92-434C>T
ENST00000306434.7:c.92-434C>T ENSP00000303147.3:n.92-434C>T
ENST00000409017.1:c.-98-434C>T ENSP00000386353.1:n.-98-434C>T
ENST00000465151.5:n.212-434C>T
ENST00000469221.5:n.212-434C>T
ENST00000481412.5:n.70-434C>T
NM_005911.5:c.92-434C>T NP_005902.1:n.92-434C>T
NM_005911.6:c.92-434C>T MANE Select NP_005902.1:n.92-434C>T
Search 100 bp 5'
Search 100 bp 3'