Canonical Allele Identifier: CA767382958
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs1386529489

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323105C>G , CM000664.2:g.27323105C>G GRCh38
NC_000002.11:g.27545972C>G , CM000664.1:g.27545972C>G GRCh37
NC_000002.10:g.27399476C>G NCBI36
NG_008075.1:g.4460G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357186.10:c.18+1328G>C ENSP00000349713.6:n.18+1328G>C
XM_005264327.2:c.-183G>C XP_005264384.1:n.-183G>C