Canonical Allele Identifier: CA1665449774
Gene:

Linked Data

dbSNP Id: rs1774560134

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398870A>G , CM000668.2:g.134398870A>G GRCh38
NC_000006.11:g.134720008A>G , CM000668.1:g.134720008A>G GRCh37
NC_000006.10:g.134761701A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428023.2:n.23+141A>G