Canonical Allele Identifier: CA2391130628

Gene:

Linked Data

• dbSNP Id: rs1985726622

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43168946T>C , CM000683.2:g.43168946T>C	GRCh38
NG_009823.1:g.4916T>C

Transcript Alleles

HGVS	Amino-acid Change
XR_001755073.1:n.647+2091A>G