Canonical Allele Identifier: CA1500737620
Gene:

Linked Data

dbSNP Id: rs1733822727

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559335G>A , CM000666.2:g.144559335G>A GRCh38
NC_000004.11:g.145480487G>A , CM000666.1:g.145480487G>A GRCh37
NC_000004.10:g.145699937G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143357C>T ENSP00000497507.1:n.328-143357C>T
XR_939272.1:n.178+2649C>T
XR_939273.1:n.178+2649C>T
XR_939272.2:n.522+2649C>T
XR_939273.2:n.522+2649C>T