Canonical Allele Identifier: CA767382984
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs1267604609
gnomAD v3: 2-27323156-G-A
gnomAD v4: 2-27323156-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323156G>A , CM000664.2:g.27323156G>A GRCh38
NC_000002.11:g.27546023G>A , CM000664.1:g.27546023G>A GRCh37
NC_000002.10:g.27399527G>A NCBI36
NG_008075.1:g.4409C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357186.10:c.18+1277C>T ENSP00000349713.6:n.18+1277C>T
XM_005264327.2:c.-234C>T XP_005264384.1:n.-234C>T