Canonical Allele Identifier: CA44473229
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs970758811
MyVariant Identifiers: chr2:g.27323165T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323165T>A , CM000664.2:g.27323165T>A GRCh38
NC_000002.11:g.27546032T>A , CM000664.1:g.27546032T>A GRCh37
NC_000002.10:g.27399536T>A NCBI36
NG_008075.1:g.4400A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357186.10:c.18+1268A>T ENSP00000349713.6:n.18+1268A>T
XM_005264327.2:c.-243A>T XP_005264384.1:n.-243A>T