Canonical Allele Identifier: CA1668053391

Gene:

Linked Data

• dbSNP Id: rs1775186854

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.140848730T>A , CM000668.2:g.140848730T>A	GRCh38
NC_000006.11:g.141169867T>A , CM000668.1:g.141169867T>A	GRCh37
NC_000006.10:g.141211560T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_428030.2:n.327-2426A>T
XR_943075.1:n.315-2426A>T
XR_943076.1:n.246-2426A>T
XR_001744390.1:n.235-32500A>T
XR_428030.4:n.341-2426A>T
XR_943075.3:n.329-2426A>T