Canonical Allele Identifier: CA2260478500
Gene:

Linked Data

dbSNP Id: rs2085621356

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42430296A>G , CM000679.2:g.42430296A>G GRCh38
NC_000017.10:g.40582314A>G , CM000679.1:g.40582314A>G GRCh37
NC_000017.9:g.37835840A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934762.1:n.505+5234A>G
XR_934763.1:n.423+5234A>G
XR_934765.1:n.255+5234A>G
XR_001752890.2:n.326+5234A>G
XR_002958124.1:n.382-5970A>G
XR_934762.2:n.553+5234A>G
XR_934765.2:n.257+5234A>G