Canonical Allele Identifier: CA2391130635
Gene:

Linked Data

dbSNP Id: rs1026439128

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43168959C>T , CM000683.2:g.43168959C>T GRCh38
NG_009823.1:g.4929C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001755073.1:n.647+2078G>A