Canonical Allele Identifier: CA323577563
Gene:

Linked Data

dbSNP Id: rs906275436

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36129832C>A , CM000684.2:g.36129832C>A GRCh38
NC_000022.10:g.36525880C>A , CM000684.1:g.36525880C>A GRCh37
NC_000022.9:g.34855826C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_430441.2:n.1547+3330G>T
XR_938219.1:n.3104G>T
XR_938220.1:n.3104G>T
XR_938221.1:n.1471+4030G>T
XR_001755516.2:n.4966G>T
XR_001755517.2:n.3193G>T
XR_001755518.2:n.4966G>T
XR_001755519.2:n.4966G>T
XR_001755520.2:n.4966G>T
XR_001755521.2:n.4966G>T
XR_001755522.2:n.1637-2059G>T
XR_001755525.2:n.1637-478G>T
XR_001755526.2:n.1637-2059G>T
XR_430441.4:n.1636+3330G>T