Canonical Allele Identifier: CA2654731370
Gene:

Linked Data

dbSNP Id: rs1985726784

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43168957C>T , CM000683.2:g.43168957C>T GRCh38
NG_009823.1:g.4927C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001755073.1:n.647+2080G>A