Canonical Allele Identifier: CA1247519140
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534677G= , CM000664.2:g.41534677G= GRCh38
NC_000002.11:g.41761817G= , CM000664.1:g.41761817G= GRCh37
NC_000002.10:g.41615321G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3049C=
XR_939997.1:n.146+3049C=
XR_939997.2:n.9529+3049C=