Canonical Allele Identifier: CA1760507362

Gene:

Linked Data

• dbSNP Id: rs1798568216

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5906949G>A , CM000670.2:g.5906949G>A	GRCh38
NC_000008.10:g.5764471G>A , CM000670.1:g.5764471G>A	GRCh37
NC_000008.9:g.5751879G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7218C>T
XR_941375.1:n.308-7218C>T
XR_941376.1:n.406-7218C>T
XR_941377.1:n.308-7218C>T
XR_941378.1:n.216-7218C>T
XR_001745765.1:n.308-7218C>T
XR_001745766.1:n.406-7218C>T
XR_001745767.1:n.216-7218C>T
XR_001745768.1:n.308-7218C>T
XR_941374.2:n.308-7218C>T
XR_941375.2:n.308-7218C>T