Canonical Allele Identifier: CA14994399
Gene:

Linked Data

dbSNP Id: rs1476029

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36121884C>T , CM000684.2:g.36121884C>T GRCh38
NC_000022.10:g.36517932C>T , CM000684.1:g.36517932C>T GRCh37
NC_000022.9:g.34847878C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_430441.2:n.1548-189G>A
XR_938221.1:n.1472-189G>A
XR_001755516.2:n.5118-189G>A
XR_001755517.2:n.4060-189G>A
XR_001755522.2:n.2483-189G>A
XR_001755525.2:n.1824-189G>A
XR_430441.4:n.1637-189G>A