Canonical Allele Identifier: CA323577645
Gene:

Linked Data

dbSNP Id: rs12166657

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36130033C>T , CM000684.2:g.36130033C>T GRCh38
NC_000022.10:g.36526081C>T , CM000684.1:g.36526081C>T GRCh37
NC_000022.9:g.34856027C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_430441.2:n.1547+3129G>A
XR_938219.1:n.2903G>A
XR_938220.1:n.2903G>A
XR_938221.1:n.1471+3829G>A
XR_001755516.2:n.4765G>A
XR_001755517.2:n.2992G>A
XR_001755518.2:n.4765G>A
XR_001755519.2:n.4765G>A
XR_001755520.2:n.4765G>A
XR_001755521.2:n.4765G>A
XR_001755522.2:n.1637-2260G>A
XR_001755525.2:n.1637-679G>A
XR_001755526.2:n.1637-2260G>A
XR_430441.4:n.1636+3129G>A