Canonical Allele Identifier: CA1687788268
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.10667229G= , CM000669.2:g.10667229G= GRCh38
NC_000007.13:g.10706856G= , CM000669.1:g.10706856G= GRCh37
NC_000007.12:g.10673381G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147499.1:n.64-105652C=
XR_001745090.1:n.376-8067G=