Canonical Allele Identifier: CA2838674967
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837464T>C , CM000681.2:g.50837464T>C GRCh38
NC_000019.9:g.51340720T>C , CM000681.1:g.51340720T>C GRCh37
NC_000019.8:g.56032532T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6171T>C
NR_131205.1:n.230+6171T>C
XR_936030.1:n.298+6171T>C
XR_936031.1:n.298+6171T>C
XR_936032.1:n.298+6171T>C
XR_936033.1:n.294+6171T>C
XR_936035.1:n.281+6171T>C