Canonical Allele Identifier: CA1687788262
Gene:

Linked Data

dbSNP Id: rs1779982552

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.10667224T>C , CM000669.2:g.10667224T>C GRCh38
NC_000007.13:g.10706851T>C , CM000669.1:g.10706851T>C GRCh37
NC_000007.12:g.10673376T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147499.1:n.64-105647A>G
XR_001745090.1:n.376-8072T>C