Canonical Allele Identifier: CA1502607191
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748325C= , CM000666.2:g.148748325C= GRCh38
NC_000004.11:g.149669477C= , CM000666.1:g.149669477C= GRCh37
NC_000004.10:g.149888927C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741441.1:n.1746-118432C=