Canonical Allele Identifier: CA1674890195
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817554C= , CM000668.2:g.155817554C= GRCh38
NC_000006.11:g.156138688C= , CM000668.1:g.156138688C= GRCh37
NC_000006.10:g.156180380C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+24135C=
XR_943146.1:n.552-2884G=
XR_001744423.1:n.606-2884G=
XR_001744424.1:n.79+24135C=