Canonical Allele Identifier: CA752803753
Gene:

Linked Data

dbSNP Id: rs1264479774

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36130026T>C , CM000684.2:g.36130026T>C GRCh38
NC_000022.10:g.36526074T>C , CM000684.1:g.36526074T>C GRCh37
NC_000022.9:g.34856020T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_430441.2:n.1547+3136A>G
XR_938219.1:n.2910A>G
XR_938220.1:n.2910A>G
XR_938221.1:n.1471+3836A>G
XR_001755516.2:n.4772A>G
XR_001755517.2:n.2999A>G
XR_001755518.2:n.4772A>G
XR_001755519.2:n.4772A>G
XR_001755520.2:n.4772A>G
XR_001755521.2:n.4772A>G
XR_001755522.2:n.1637-2253A>G
XR_001755525.2:n.1637-672A>G
XR_001755526.2:n.1637-2253A>G
XR_430441.4:n.1636+3136A>G