Canonical Allele Identifier: CA2658328704
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs1186714597
gnomAD v4: 2-27323252-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323252A>C , CM000664.2:g.27323252A>C GRCh38
NC_000002.11:g.27546119A>C , CM000664.1:g.27546119A>C GRCh37
NC_000002.10:g.27399623A>C NCBI36
NG_008075.1:g.4313T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357186.10:c.18+1181T>G ENSP00000349713.6:n.18+1181T>G
XM_005264327.2:c.-330T>G XP_005264384.1:n.-330T>G