Canonical Allele Identifier: CA2273295140
Gene:

Linked Data

dbSNP Id: rs1905462455

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70831996C>T , CM000679.2:g.70831996C>T GRCh38
NC_000017.10:g.68828137C>T , CM000679.1:g.68828137C>T GRCh37
NC_000017.9:g.66339732C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934956.1:n.62+3218G>A
XR_934956.2:n.114+3218G>A