Canonical Allele Identifier: CA15465836
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105812253A>G , CM000668.2:g.105812253A>G GRCh38
NC_000006.11:g.106260128A>G , CM000668.1:g.106260128A>G GRCh37
NC_000006.10:g.106366821A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942835.1:n.510+17804T>C
XR_001744274.1:n.438+17804T>C
XR_001744275.1:n.337+17804T>C