Canonical Allele Identifier: CA1266821822

Gene: MAT2A

Linked Data

• dbSNP Id: rs1691447568

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85540517C>G , CM000664.2:g.85540517C>G	GRCh38
NC_000002.11:g.85767640C>G , CM000664.1:g.85767640C>G	GRCh37
NC_000002.10:g.85621151C>G	NCBI36
NG_029183.1:g.6540C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000306434.8:c.92-566C>G MANE Select	ENSP00000303147.3:n.92-566C>G
ENST00000306434.7:c.92-566C>G	ENSP00000303147.3:n.92-566C>G
ENST00000409017.1:c.-99+517C>G	ENSP00000386353.1:n.-99+517C>G
ENST00000465151.5:n.212-566C>G
ENST00000469221.5:n.212-566C>G
ENST00000481412.5:n.70-566C>G
NM_005911.5:c.92-566C>G	NP_005902.1:n.92-566C>G
NM_005911.6:c.92-566C>G MANE Select	NP_005902.1:n.92-566C>G