Canonical Allele Identifier: CA1653130401
Gene:

Linked Data

dbSNP Id: rs1771941618

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805178G>T , CM000668.2:g.105805178G>T GRCh38
NC_000006.11:g.106253053G>T , CM000668.1:g.106253053G>T GRCh37
NC_000006.10:g.106359746G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24879C>A
XR_001744274.1:n.438+24879C>A
XR_001744275.1:n.337+24879C>A