Canonical Allele Identifier: CA12254308
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs17827966

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817575T>C , CM000668.2:g.155817575T>C GRCh38
NC_000006.11:g.156138709T>C , CM000668.1:g.156138709T>C GRCh37
NC_000006.10:g.156180401T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24156T>C
XR_943146.1:n.552-2905A>G
XR_001744423.1:n.606-2905A>G
XR_001744424.1:n.79+24156T>C