Canonical Allele Identifier: CA1638624360
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.74448571T= , CM000668.2:g.74448571T= GRCh38
NC_000006.11:g.75158287T= , CM000668.1:g.75158287T= GRCh37
NC_000006.10:g.75215007T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110856.1:n.193+101442T=