Canonical Allele Identifier: CA1760508112

Gene:

Linked Data

• dbSNP Id: rs1798589131

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907838T>C , CM000670.2:g.5907838T>C	GRCh38
NC_000008.10:g.5765360T>C , CM000670.1:g.5765360T>C	GRCh37
NC_000008.9:g.5752768T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-8107A>G
XR_941375.1:n.308-8107A>G
XR_941376.1:n.406-8107A>G
XR_941377.1:n.308-8107A>G
XR_941378.1:n.216-8107A>G
XR_001745765.1:n.308-8107A>G
XR_001745766.1:n.406-8107A>G
XR_001745767.1:n.216-8107A>G
XR_001745768.1:n.308-8107A>G
XR_941374.2:n.308-8107A>G
XR_941375.2:n.308-8107A>G