Canonical Allele Identifier: CA2530245487
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812462T>C , CM000668.2:g.155812462T>C GRCh38
NC_000006.11:g.156133596T>C , CM000668.1:g.156133596T>C GRCh37
NC_000006.10:g.156175288T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19043T>C
XR_943146.1:n.645-423A>G
XR_001744423.1:n.699-423A>G
XR_001744424.1:n.79+19043T>C