Canonical Allele Identifier: CA2581614818
Gene:

Genomic Alleles

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

Transcript Alleles

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