Canonical Allele Identifier: CA2330336186
Gene:

Linked Data

dbSNP Id: rs2011163851

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544487A>C , CM000681.2:g.28544487A>C GRCh38
NC_000019.9:g.29035394A>C , CM000681.1:g.29035394A>C GRCh37
NC_000019.8:g.33727234A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-77707T>G
XR_243979.1:n.110-51464T>G