Canonical Allele Identifier: CA2330336288
Gene:

Linked Data

dbSNP Id: rs2011164814

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544663A>C , CM000681.2:g.28544663A>C GRCh38
NC_000019.9:g.29035570A>C , CM000681.1:g.29035570A>C GRCh37
NC_000019.8:g.33727410A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77883T>G
XR_243979.1:n.110-51640T>G