Canonical Allele Identifier: CA1240221796
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs1679916291
gnomAD v4: 2-27323104-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323104A>G , CM000664.2:g.27323104A>G GRCh38
NC_000002.11:g.27545971A>G , CM000664.1:g.27545971A>G GRCh37
NC_000002.10:g.27399475A>G NCBI36
NG_008075.1:g.4461T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357186.10:c.18+1329T>C ENSP00000349713.6:n.18+1329T>C
XM_005264327.2:c.-182T>C XP_005264384.1:n.-182T>C