Canonical Allele Identifier: CA1657688893
Gene:

Linked Data

dbSNP Id: rs1776571678

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450219T>C , CM000668.2:g.117450219T>C GRCh38
NC_000006.11:g.117771382T>C , CM000668.1:g.117771382T>C GRCh37
NC_000006.10:g.117878075T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116635A>G ENSP00000487717.1:n.547+116635A>G