Canonical Allele Identifier: CA1247518966
Gene:

Linked Data

dbSNP Id: rs982288220

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534414A>C , CM000664.2:g.41534414A>C GRCh38
NC_000002.11:g.41761554A>C , CM000664.1:g.41761554A>C GRCh37
NC_000002.10:g.41615058A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+3312T>G
XR_939997.1:n.146+3312T>G
XR_939997.2:n.9529+3312T>G