Canonical Allele Identifier: CA1610684691

Gene:

Linked Data

• dbSNP Id: rs1766138952

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.11943326A>G , CM000668.2:g.11943326A>G	GRCh38
NC_000006.11:g.11943559A>G , CM000668.1:g.11943559A>G	GRCh37
NC_000006.10:g.12051545A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743976.1:n.348-8209A>G