Canonical Allele Identifier: CA112548366
Gene: F11-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs529590575

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186417130T>C , CM000666.2:g.186417130T>C GRCh38
NC_000004.11:g.187338284T>C , CM000666.1:g.187338284T>C GRCh37
NC_000004.10:g.187575278T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033900.1:n.214+83715A>G
XR_427648.2:n.1186-794A>G
XR_939587.1:n.1354-794A>G
XR_939588.1:n.1074-794A>G
NR_033901.2:n.1573-794A>G