Canonical Allele Identifier: CA2705075280
Gene:

Linked Data

dbSNP Id: rs1577128570

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578339C>T , CM000666.2:g.12578339C>T GRCh38
NC_000004.11:g.12579963C>T , CM000666.1:g.12579963C>T GRCh37
NC_000004.10:g.12189061C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31003G>A
XR_001741374.1:n.254+44316G>A
XR_925406.3:n.140+31003G>A