Canonical Allele Identifier: CA767383060
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs1323660408
gnomAD v3: 2-27323206-G-A
gnomAD v4: 2-27323206-G-A
MyVariant Identifiers: chr2:g.27546073G>A (hg19) chr2:g.27323206G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27323206G>A , CM000664.2:g.27323206G>A GRCh38
NC_000002.11:g.27546073G>A , CM000664.1:g.27546073G>A GRCh37
NC_000002.10:g.27399577G>A NCBI36
NG_008075.1:g.4359C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357186.10:c.18+1227C>T ENSP00000349713.6:n.18+1227C>T
XM_005264327.2:c.-284C>T XP_005264384.1:n.-284C>T
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