Canonical Allele Identifier: CA1786774838
Gene:

Linked Data

dbSNP Id: rs1585767085

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.57928336A>C , CM000670.2:g.57928336A>C GRCh38
NC_000008.10:g.58840895A>C , CM000670.1:g.58840895A>C GRCh37
NC_000008.9:g.59003449A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928921.1:n.347-29940A>C
XR_928921.2:n.349-29940A>C