Canonical Allele Identifier: CA767383055

Gene: MPV17

Linked Data

• dbSNP Id: rs1441587256
• gnomAD v3: 2-27323204-C-T
• gnomAD v4: 2-27323204-C-T
• MyVariant Identifiers: chr2:g.27546071C>T (hg19) ; chr2:g.27323204C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27323204C>T , CM000664.2:g.27323204C>T	GRCh38
NC_000002.11:g.27546071C>T , CM000664.1:g.27546071C>T	GRCh37
NC_000002.10:g.27399575C>T	NCBI36
NG_008075.1:g.4361G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357186.10:c.18+1229G>A	ENSP00000349713.6:n.18+1229G>A
XM_005264327.2:c.-282G>A	XP_005264384.1:n.-282G>A