Canonical Allele Identifier: CA1749618117
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.145144363T= , CM000669.2:g.145144363T= GRCh38
NC_000007.13:g.144841456T= , CM000669.1:g.144841456T= GRCh37
NC_000007.12:g.144472389T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928090.1:n.1968-12572T=
XR_928090.2:n.4143-12572T=