Canonical Allele Identifier: CA1266821828
Gene: MAT2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540520A= , CM000664.2:g.85540520A= GRCh38
NC_000002.11:g.85767643A= , CM000664.1:g.85767643A= GRCh37
NC_000002.10:g.85621154A= NCBI36
NG_029183.1:g.6543A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306434.8:c.92-563A= MANE Select ENSP00000303147.3:n.92-563A=
ENST00000306434.7:c.92-563A= ENSP00000303147.3:n.92-563A=
ENST00000409017.1:c.-99+520A= ENSP00000386353.1:n.-99+520A=
ENST00000465151.5:n.212-563A=
ENST00000469221.5:n.212-563A=
ENST00000481412.5:n.70-563A=
NM_005911.5:c.92-563A= NP_005902.1:n.92-563A=
NM_005911.6:c.92-563A= MANE Select NP_005902.1:n.92-563A=
Search 100 bp 5'
Search 100 bp 3'