Canonical Allele Identifier: CA1751418959
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807194T= , CM000669.2:g.148807194T= GRCh38
NC_000007.13:g.148504286T= , CM000669.1:g.148504286T= GRCh37
NC_000007.12:g.148135219T= NCBI36
NG_032043.1:g.82156A= , LRG_531:g.82156A=

Transcript Alleles

HGVS Amino-acid Change
XR_928101.1:n.515+2109T=
XR_928102.1:n.722+2109T=