Canonical Allele Identifier: CA1657688870
Gene:

Linked Data

dbSNP Id: rs1582939952

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450188A>C , CM000668.2:g.117450188A>C GRCh38
NC_000006.11:g.117771351A>C , CM000668.1:g.117771351A>C GRCh37
NC_000006.10:g.117878044A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000467125.1:c.547+116666T>G ENSP00000487717.1:n.547+116666T>G