Canonical Allele Identifier: CA1818161764
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012592C= , CM000670.2:g.127012592C= GRCh38
NC_000008.10:g.128024837C= , CM000670.1:g.128024837C= GRCh37
NC_000008.9:g.128094019C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1364+5974C=