Canonical Allele Identifier: CA2391130637

Gene:

Linked Data

• dbSNP Id: rs1985727124

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43168969G>A , CM000683.2:g.43168969G>A	GRCh38
NG_009823.1:g.4939G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_001755073.1:n.647+2068C>T