Canonical Allele Identifier: CA1649549855
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98128362C= , CM000668.2:g.98128362C= GRCh38
NC_000006.11:g.98576238C= , CM000668.1:g.98576238C= GRCh37
NC_000006.10:g.98682959C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942809.1:n.456+29092C=