Canonical Allele Identifier: CA1247519176
Gene:

Linked Data

dbSNP Id: rs1667992421

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534731T>C , CM000664.2:g.41534731T>C GRCh38
NC_000002.11:g.41761871T>C , CM000664.1:g.41761871T>C GRCh37
NC_000002.10:g.41615375T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+2995A>G
XR_939997.1:n.146+2995A>G
XR_939997.2:n.9529+2995A>G