Canonical Allele Identifier: CA16095889
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10865170

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534660C>A , CM000664.2:g.41534660C>A GRCh38
NC_000002.10:g.41615304C>A NCBI36
NC_000002.11:g.41761800C>A , CM000664.1:g.41761800C>A GRCh37

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3066G>T
XR_939997.1:n.146+3066G>T
XR_939997.2:n.9529+3066G>T