Canonical Allele Identifier: CA1247519134
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534673T= , CM000664.2:g.41534673T= GRCh38
NC_000002.11:g.41761813T= , CM000664.1:g.41761813T= GRCh37
NC_000002.10:g.41615317T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3053A=
XR_939997.1:n.146+3053A=
XR_939997.2:n.9529+3053A=