Canonical Allele Identifier: CA2661421941
Gene: MMADHC HGNC NCBI

Linked Data

gnomAD v4: 2-149569643-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.149569643C>A , CM000664.2:g.149569643C>A GRCh38
NC_000002.11:g.150426157C>A , CM000664.1:g.150426157C>A GRCh37
NC_000002.10:g.150134403C>A NCBI36
NG_009189.1:g.23174G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000303319.10:c.*331G>T MANE Select ENSP00000301920.5:n.*331G>T
ENST00000303319.9:c.*331G>T ENSP00000301920.5:n.*331G>T
NM_015702.2:c.*331G>T NP_056517.1:n.*331G>T
NM_015702.3:c.*331G>T MANE Select NP_056517.1:n.*331G>T
Search 100 bp 5'
Search 100 bp 3'