Canonical Allele Identifier: CA1439212811
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578186T= , CM000666.2:g.12578186T= GRCh38
NC_000004.11:g.12579810T= , CM000666.1:g.12579810T= GRCh37
NC_000004.10:g.12188908T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31156A=
XR_001741374.1:n.254+44469A=
XR_925406.3:n.140+31156A=