Canonical Allele Identifier: CA1247519105
Gene:

Linked Data

dbSNP Id: rs1049765226

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534634T>C , CM000664.2:g.41534634T>C GRCh38
NC_000002.11:g.41761774T>C , CM000664.1:g.41761774T>C GRCh37
NC_000002.10:g.41615278T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3092A>G
XR_939997.1:n.146+3092A>G
XR_939997.2:n.9529+3092A>G