Canonical Allele Identifier: CA1510999052
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.167343098C= , CM000666.2:g.167343098C= GRCh38
NC_000004.11:g.168264249C= , CM000666.1:g.168264249C= GRCh37
NC_000004.10:g.168500824C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939421.1:n.217-34311G=