Canonical Allele Identifier: CA1025451874
Gene:

Linked Data

dbSNP Id: rs2059867836

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36129854T>C , CM000684.2:g.36129854T>C GRCh38
NC_000022.10:g.36525902T>C , CM000684.1:g.36525902T>C GRCh37
NC_000022.9:g.34855848T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_430441.2:n.1547+3308A>G
XR_938219.1:n.3082A>G
XR_938220.1:n.3082A>G
XR_938221.1:n.1471+4008A>G
XR_001755516.2:n.4944A>G
XR_001755517.2:n.3171A>G
XR_001755518.2:n.4944A>G
XR_001755519.2:n.4944A>G
XR_001755520.2:n.4944A>G
XR_001755521.2:n.4944A>G
XR_001755522.2:n.1637-2081A>G
XR_001755525.2:n.1637-500A>G
XR_001755526.2:n.1637-2081A>G
XR_430441.4:n.1636+3308A>G