Canonical Allele Identifier: CA2581614814
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805124T>A , CM000668.2:g.105805124T>A GRCh38
NC_000006.11:g.106252999T>A , CM000668.1:g.106252999T>A GRCh37
NC_000006.10:g.106359692T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24933A>T
XR_001744274.1:n.438+24933A>T
XR_001744275.1:n.337+24933A>T