Canonical Allele Identifier: CA1500738041
Gene:

Linked Data

dbSNP Id: rs1733830571

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559746C>A , CM000666.2:g.144559746C>A GRCh38
NC_000004.11:g.145480898C>A , CM000666.1:g.145480898C>A GRCh37
NC_000004.10:g.145700348C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143768G>T ENSP00000497507.1:n.328-143768G>T
XR_939272.1:n.178+2238G>T
XR_939273.1:n.178+2238G>T
XR_939272.2:n.522+2238G>T
XR_939273.2:n.522+2238G>T