Canonical Allele Identifier: CA2713322856
Gene:

Linked Data

dbSNP Id: rs2114700381

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817700T>C , CM000668.2:g.155817700T>C GRCh38
NC_000006.11:g.156138834T>C , CM000668.1:g.156138834T>C GRCh37
NC_000006.10:g.156180526T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24281T>C
XR_943146.1:n.552-3030A>G
XR_001744423.1:n.606-3030A>G
XR_001744424.1:n.79+24281T>C