Canonical Allele Identifier: CA820839142
Gene:

Linked Data

dbSNP Id: rs1396195557

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633459C>G , CM000668.2:g.151633459C>G GRCh38
NC_000006.11:g.151954594C>G , CM000668.1:g.151954594C>G GRCh37
NC_000006.10:g.151996287C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3477C>G