ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA328084835
Gene: VKORC1P1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.27863980G>T
GRCh37
chrX:g.27882097G>T
Linked Data - Sequence & Population
gnomAD v4:
chrX-27863980-G-T
Linked Data - NCBI & NCI
dbSNP:
28940302
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.27863980G>T , CM000685.2:g.27863980G>T
GRCh38
NC_000023.10:g.27882097G>T , CM000685.1:g.27882097G>T
GRCh37
NC_000023.9:g.27792018G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000421897.1:n.88G>T
Search 100 bp 5'
Search 100 bp 3'