Canonical Allele Identifier: CA1605276916
Gene:

Linked Data

dbSNP Id: rs1762570082

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465986G>T , CM000668.2:g.465986G>T GRCh38
NC_000006.11:g.465986G>T , CM000668.1:g.465986G>T GRCh37
NC_000006.10:g.410986G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926364.1:n.2714+12261G>T
XR_926365.1:n.2548+12261G>T
XR_001743914.1:n.482-9222G>T