Canonical Allele Identifier: CA2604171736
Gene:

Linked Data

dbSNP Id: rs2104659826

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884065A>C , CM000664.2:g.122884065A>C GRCh38
NC_000002.11:g.123641641A>C , CM000664.1:g.123641641A>C GRCh37
NC_000002.10:g.123358111A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-877A>C
XR_001739692.1:n.1451-877A>C
XR_923292.2:n.1358-877A>C