Canonical Allele Identifier: CA2330336172
Gene:

Linked Data

dbSNP Id: rs763609453

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544456A>C , CM000681.2:g.28544456A>C GRCh38
NC_000019.9:g.29035363A>C , CM000681.1:g.29035363A>C GRCh37
NC_000019.8:g.33727203A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-77676T>G
XR_243979.1:n.110-51433T>G