Canonical Allele Identifier: CA112548362

Gene: F11-AS1

Linked Data

• dbSNP Id: rs969506767
• gnomAD v2: 4-187338274-C-T
• gnomAD v3: 4-186417120-C-T
• gnomAD v4: 4-186417120-C-T
• MyVariant Identifiers: chr4:g.187338274C>T (hg19) ; chr4:g.186417120C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186417120C>T , CM000666.2:g.186417120C>T	GRCh38
NC_000004.11:g.187338274C>T , CM000666.1:g.187338274C>T	GRCh37
NC_000004.10:g.187575268C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033900.1:n.214+83725G>A
XR_427648.2:n.1186-784G>A
XR_939587.1:n.1354-784G>A
XR_939588.1:n.1074-784G>A
NR_033901.2:n.1573-784G>A