Canonical Allele Identifier: CA2550368785
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43168994C>T , CM000683.2:g.43168994C>T GRCh38
NG_009823.1:g.4964C>T

Transcript Alleles

HGVS Amino-acid Change
XR_001755073.1:n.647+2043G>A