Canonical Allele Identifier: CA15113044
Gene:

Linked Data

dbSNP Id: rs12068654

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160773959T>G , CM000663.2:g.160773959T>G GRCh38
NC_000001.10:g.160743749T>G , CM000663.1:g.160743749T>G GRCh37
NC_000001.9:g.159010373T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922204.1:n.2774A>C
XR_922205.1:n.2670A>C
XR_922206.1:n.786-27A>C
XR_001738267.1:n.698-27A>C
XR_922205.2:n.2686A>C