Canonical Allele Identifier: CA1286885899
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431553G= , CM000664.2:g.127431553G= GRCh38
NC_000002.11:g.128189129G= , CM000664.1:g.128189129G= GRCh37
NC_000002.10:g.127905599G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923313.1:n.1331+114C=
XR_001739705.1:n.3607-3289C=
XR_923313.2:n.4042+114C=