Canonical Allele Identifier: CA1610684745
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943385A= , CM000668.2:g.11943385A= GRCh38
NC_000006.11:g.11943618A= , CM000668.1:g.11943618A= GRCh37
NC_000006.10:g.12051604A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-8150A=