Canonical Allele Identifier: CA1240221810
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs556165748
gnomAD v4: 2-27323130-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323130T>A , CM000664.2:g.27323130T>A GRCh38
NC_000002.11:g.27545997T>A , CM000664.1:g.27545997T>A GRCh37
NC_000002.10:g.27399501T>A NCBI36
NG_008075.1:g.4435A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357186.10:c.18+1303A>T ENSP00000349713.6:n.18+1303A>T
XM_005264327.2:c.-208A>T XP_005264384.1:n.-208A>T