Canonical Allele Identifier: CA1775343102
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808230A= , CM000670.2:g.33808230A= GRCh38
NC_000008.10:g.33665748A= , CM000670.1:g.33665748A= GRCh37
NC_000008.9:g.33785290A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949659.1:n.240+11794A=
XR_002956701.1:n.240+11794A=