Canonical Allele Identifier: CA2838373603
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156314917T>C , CM000668.2:g.156314917T>C GRCh38
NC_000006.11:g.156636051T>C , CM000668.1:g.156636051T>C GRCh37
NC_000006.10:g.156677743T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943138.1:n.206+3157T>C
XR_943139.1:n.206+3157T>C
XR_943140.1:n.206+3157T>C
XR_943141.1:n.115+3862T>C
XR_943146.1:n.19-20163A>G
XR_943136.2:n.504+3862T>C
XR_943139.2:n.595+3157T>C
XR_943140.2:n.595+3157T>C