Canonical Allele Identifier: CA165047078
Gene:

Linked Data

dbSNP Id: rs970603836

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.112988350A>G , CM000669.2:g.112988350A>G GRCh38
NC_000007.13:g.112628405A>G , CM000669.1:g.112628405A>G GRCh37
NC_000007.12:g.112415641A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110162.1:n.77-1686T>C