Canonical Allele Identifier: CA1008414856
Gene:

Linked Data

dbSNP Id: rs6427595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161493708G>T , CM000663.2:g.161493708G>T GRCh38
NC_000001.10:g.161463498G>T , CM000663.1:g.161463498G>T GRCh37
NC_000001.9:g.159730122G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922214.1:n.2011+89G>T
XR_922214.2:n.2960+89G>T