Canonical Allele Identifier: CA348868701
Gene: MMADHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.150426499T>C (hg19) chr2:g.149569985T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149569985T>C , CM000664.2:g.149569985T>C GRCh38
NC_000002.11:g.150426499T>C , CM000664.1:g.150426499T>C GRCh37
NC_000002.10:g.150134745T>C NCBI36
NG_009189.1:g.22832A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.880A>G MANE Select ENSP00000301920.5:p.Ser294Gly
ENST00000303319.9:c.880A>G ENSP00000301920.5:p.Ser294Gly
ENST00000422782.2:c.982A>G ENSP00000408331.2:p.Ser328Gly
ENST00000428879.5:c.880A>G ENSP00000389060.1:p.Ser294Gly
NM_015702.2:c.880A>G NP_056517.1:p.Ser294Gly
NM_015702.3:c.880A>G MANE Select NP_056517.1:p.Ser294Gly
Search 100 bp 5'
Search 100 bp 3'