Canonical Allele Identifier: CA2138728381
Community Standard Title: NC_000014.9:g.55951401G=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.55951401G= , CM000676.2:g.55951401G= GRCh38
NC_000014.8:g.56418119G= , CM000676.1:g.56418119G= GRCh37
NC_000014.7:g.55487872G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001750770.1:n.364-6561G=
XR_429364.2:n.164-6561G=
XR_943897.1:n.164-6561G=