Canonical Allele Identifier: CA1500737636
Gene:

Linked Data

dbSNP Id: rs1733823234

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559354C>A , CM000666.2:g.144559354C>A GRCh38
NC_000004.11:g.145480506C>A , CM000666.1:g.145480506C>A GRCh37
NC_000004.10:g.145699956C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143376G>T ENSP00000497507.1:n.328-143376G>T
XR_939272.1:n.178+2630G>T
XR_939273.1:n.178+2630G>T
XR_939272.2:n.522+2630G>T
XR_939273.2:n.522+2630G>T