Canonical Allele Identifier: CA307005679
Gene:

Linked Data

dbSNP Id: rs908110711

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544587A>C , CM000681.2:g.28544587A>C GRCh38
NC_000019.9:g.29035494A>C , CM000681.1:g.29035494A>C GRCh37
NC_000019.8:g.33727334A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-77807T>G
XR_243979.1:n.110-51564T>G