Canonical Allele Identifier: CA58332357
Gene: MMADHC HGNC NCBI

Linked Data

dbSNP Id: rs895880527

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149570091G>T , CM000664.2:g.149570091G>T GRCh38
NC_000002.11:g.150426605G>T , CM000664.1:g.150426605G>T GRCh37
NC_000002.10:g.150134851G>T NCBI36
NG_009189.1:g.22726C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000303319.10:c.774C>A MANE Select ENSP00000301920.5:p.Asp258Glu
ENST00000303319.9:c.774C>A ENSP00000301920.5:p.Asp258Glu
ENST00000422782.2:c.876C>A ENSP00000408331.2:p.Asp292Glu
ENST00000428879.5:c.774C>A ENSP00000389060.1:p.Asp258Glu
NM_015702.2:c.774C>A NP_056517.1:p.Asp258Glu
NM_015702.3:c.774C>A MANE Select NP_056517.1:p.Asp258Glu