Canonical Allele Identifier: CA1657688809
Gene:

Linked Data

dbSNP Id: rs1776568679

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450044G>T , CM000668.2:g.117450044G>T GRCh38
NC_000006.11:g.117771207G>T , CM000668.1:g.117771207G>T GRCh37
NC_000006.10:g.117877900G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116810C>A ENSP00000487717.1:n.547+116810C>A