Canonical Allele Identifier: CA2710978161
Gene:

Linked Data

dbSNP Id: rs2113482273

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943655G>A , CM000668.2:g.11943655G>A GRCh38
NC_000006.11:g.11943888G>A , CM000668.1:g.11943888G>A GRCh37
NC_000006.10:g.12051874G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7880G>A