Canonical Allele Identifier: CA1663384866
Gene:

Linked Data

dbSNP Id: rs9375674

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129895365A>C , CM000668.2:g.129895365A>C GRCh38
NC_000006.11:g.130216510A>C , CM000668.1:g.130216510A>C GRCh37
NC_000006.10:g.130258203A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942986.1:n.355+7292A>C
XR_942986.2:n.355+7292A>C