Canonical Allele Identifier: CA429405861
Gene: MMADHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.150426518G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149570004G>A , CM000664.2:g.149570004G>A GRCh38
NC_000002.11:g.150426518G>A , CM000664.1:g.150426518G>A GRCh37
NC_000002.10:g.150134764G>A NCBI36
NG_009189.1:g.22813C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.861C>T MANE Select ENSP00000301920.5:p.Ser287=
ENST00000303319.9:c.861C>T ENSP00000301920.5:p.Ser287=
ENST00000422782.2:c.963C>T ENSP00000408331.2:p.Ser321=
ENST00000428879.5:c.861C>T ENSP00000389060.1:p.Ser287=
NM_015702.2:c.861C>T NP_056517.1:p.Ser287=
NM_015702.3:c.861C>T MANE Select NP_056517.1:p.Ser287=