Canonical Allele Identifier: CA1247519181
Gene:

Linked Data

dbSNP Id: rs983510504

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534740T>C , CM000664.2:g.41534740T>C GRCh38
NC_000002.11:g.41761880T>C , CM000664.1:g.41761880T>C GRCh37
NC_000002.10:g.41615384T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+2986A>G
XR_939997.1:n.146+2986A>G
XR_939997.2:n.9529+2986A>G