Canonical Allele Identifier: CA2773674432
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817718C>T , CM000668.2:g.155817718C>T GRCh38
NC_000006.11:g.156138852C>T , CM000668.1:g.156138852C>T GRCh37
NC_000006.10:g.156180544C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+24299C>T
XR_943146.1:n.552-3048G>A
XR_001744423.1:n.606-3048G>A
XR_001744424.1:n.79+24299C>T