Canonical Allele Identifier: CA1266821854
Gene: MAT2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85540545A= , CM000664.2:g.85540545A= GRCh38
NC_000002.11:g.85767668A= , CM000664.1:g.85767668A= GRCh37
NC_000002.10:g.85621179A= NCBI36
NG_029183.1:g.6568A=

Transcript Alleles

HGVS Amino-acid change
ENST00000306434.8:c.92-538A= MANE Select ENSP00000303147.3:n.92-538A=
ENST00000306434.7:c.92-538A= ENSP00000303147.3:n.92-538A=
ENST00000409017.1:c.-98-538A= ENSP00000386353.1:n.-98-538A=
ENST00000465151.5:n.212-538A=
ENST00000469221.5:n.212-538A=
ENST00000481412.5:n.70-538A=
NM_005911.5:c.92-538A= NP_005902.1:n.92-538A=
NM_005911.6:c.92-538A= MANE Select NP_005902.1:n.92-538A=
Search 100 bp 5'
Search 100 bp 3'