Canonical Allele Identifier: CA2025046530
Gene:

Linked Data

dbSNP Id: rs1013661312

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961038C>T , CM000674.2:g.29961038C>T GRCh38
NC_000012.11:g.30113971C>T , CM000674.1:g.30113971C>T GRCh37
NC_000012.10:g.30005238C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-17998G>A
XR_931474.1:n.314-17998G>A
XR_931475.1:n.135-17998G>A
XR_001749060.1:n.314-17998G>A
XR_001749061.1:n.314-17998G>A