Canonical Allele Identifier: CA1284431689
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368968G= , CM000664.2:g.122368968G= GRCh38
NC_000002.11:g.123126544G= , CM000664.1:g.123126544G= GRCh37
NC_000002.10:g.122843014G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-23995G=
XR_001739684.1:n.556-23995G=