Canonical Allele Identifier: CA1751419002
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807244C= , CM000669.2:g.148807244C= GRCh38
NC_000007.13:g.148504336C= , CM000669.1:g.148504336C= GRCh37
NC_000007.12:g.148135269C= NCBI36
NG_032043.1:g.82106G= , LRG_531:g.82106G=

Transcript Alleles

HGVS Amino-acid Change
XR_928101.1:n.515+2159C=
XR_928102.1:n.722+2159C=