Canonical Allele Identifier: CA2330336304
Gene:

Linked Data

dbSNP Id: rs1599600938

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544691A>G , CM000681.2:g.28544691A>G GRCh38
NC_000019.9:g.29035598A>G , CM000681.1:g.29035598A>G GRCh37
NC_000019.8:g.33727438A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77911T>C
XR_243979.1:n.110-51668T>C