Canonical Allele Identifier: CA348869227
Gene: MMADHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.150426609T>G (hg19) chr2:g.149570095T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149570095T>G , CM000664.2:g.149570095T>G GRCh38
NC_000002.11:g.150426609T>G , CM000664.1:g.150426609T>G GRCh37
NC_000002.10:g.150134855T>G NCBI36
NG_009189.1:g.22722A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000303319.10:c.770A>C MANE Select ENSP00000301920.5:p.Asp257Ala
ENST00000303319.9:c.770A>C ENSP00000301920.5:p.Asp257Ala
ENST00000422782.2:c.872A>C ENSP00000408331.2:p.Asp291Ala
ENST00000428879.5:c.770A>C ENSP00000389060.1:p.Asp257Ala
NM_015702.2:c.770A>C NP_056517.1:p.Asp257Ala
NM_015702.3:c.770A>C MANE Select NP_056517.1:p.Asp257Ala
Search 100 bp 5'
Search 100 bp 3'