Canonical Allele Identifier: CA328084834
Gene: VKORC1P1 HGNC NCBI
MyVariant.info:
GRCh38 chrX:g.27863980G>C
GRCh37 chrX:g.27882097G>C
gnomAD v2:
X:27882097 G / C
gnomAD v3:
X:27863980 G / C
gnomAD v4:
chrX-27863980-G-C
Joint Max Group AF 0.00044583 (AFR)
Genomes Max Group AF 0.00034888 (AFR)
Exomes Max Group AF 0.00043656 (AFR)
dbSNP:
28940302
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.27863980G>C , CM000685.2:g.27863980G>C GRCh38
NC_000023.10:g.27882097G>C , CM000685.1:g.27882097G>C GRCh37
NC_000023.9:g.27792018G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000421897.1:n.88G>C
Search 100 bp 5'
Search 100 bp 3'