Canonical Allele Identifier: CA1839056686

Gene:

Linked Data

• dbSNP Id: rs1823377600

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21755988C>T , CM000671.2:g.21755988C>T	GRCh38
NC_000009.11:g.21755987C>T , CM000671.1:g.21755987C>T	GRCh37
NC_000009.10:g.21745987C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11837G>A