Canonical Allele Identifier: CA1653130395
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805161A= , CM000668.2:g.105805161A= GRCh38
NC_000006.11:g.106253036A= , CM000668.1:g.106253036A= GRCh37
NC_000006.10:g.106359729A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24896T=
XR_001744274.1:n.438+24896T=
XR_001744275.1:n.337+24896T=