Canonical Allele Identifier: CA2391130640
Gene:

Linked Data

dbSNP Id: rs1985727285

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43168974C>G , CM000683.2:g.43168974C>G GRCh38
NG_009823.1:g.4944C>G

Transcript Alleles

HGVS Amino-acid Change
XR_001755073.1:n.647+2063G>C