Canonical Allele Identifier: CA1902268
Gene: MMADHC HGNC NCBI

Linked Data

ClinVar Variation Id: 957054
ClinVar RCV Id: RCV001229965
dbSNP Id: rs773493767

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149570101G>C , CM000664.2:g.149570101G>C GRCh38
NC_000002.11:g.150426615G>C , CM000664.1:g.150426615G>C GRCh37
NC_000002.10:g.150134861G>C NCBI36
NG_009189.1:g.22716C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000303319.10:c.764C>G MANE Select ENSP00000301920.5:p.Ser255Cys
ENST00000303319.9:c.764C>G ENSP00000301920.5:p.Ser255Cys
ENST00000422782.2:c.866C>G ENSP00000408331.2:p.Ser289Cys
ENST00000428879.5:c.764C>G ENSP00000389060.1:p.Ser255Cys
NM_015702.2:c.764C>G NP_056517.1:p.Ser255Cys
NM_015702.3:c.764C>G MANE Select NP_056517.1:p.Ser255Cys