Canonical Allele Identifier: CA1734068789
Gene:

Linked Data

dbSNP Id: rs6968385

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.110407414C>A , CM000669.2:g.110407414C>A GRCh38
NC_000007.13:g.110047471C>A , CM000669.1:g.110047471C>A GRCh37
NC_000007.12:g.109834707C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744982.1:n.604+25397G>T
XR_927863.2:n.367+25397G>T