Canonical Allele Identifier: CA307005678
Gene:

Linked Data

dbSNP Id: rs926738173

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544575T>C , CM000681.2:g.28544575T>C GRCh38
NC_000019.9:g.29035482T>C , CM000681.1:g.29035482T>C GRCh37
NC_000019.8:g.33727322T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110759.1:n.657-77795A>G
XR_243979.1:n.110-51552A>G