Canonical Allele Identifier: CA817769208
Gene:

Linked Data

dbSNP Id: rs1243477842

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450043G>C , CM000668.2:g.117450043G>C GRCh38
NC_000006.11:g.117771206G>C , CM000668.1:g.117771206G>C GRCh37
NC_000006.10:g.117877899G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116811C>G ENSP00000487717.1:n.547+116811C>G