Canonical Allele Identifier: CA1439212922
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578286T= , CM000666.2:g.12578286T= GRCh38
NC_000004.11:g.12579910T= , CM000666.1:g.12579910T= GRCh37
NC_000004.10:g.12189008T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31056A=
XR_001741374.1:n.254+44369A=
XR_925406.3:n.140+31056A=