Canonical Allele Identifier: CA112548359

Gene: F11-AS1

Linked Data

• dbSNP Id: rs369818614
• gnomAD v2: 4-187338250-G-A
• gnomAD v3: 4-186417096-G-A
• gnomAD v4: 4-186417096-G-A
• MyVariant Identifiers: chr4:g.187338250G>A (hg19) ; chr4:g.186417096G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186417096G>A , CM000666.2:g.186417096G>A	GRCh38
NC_000004.11:g.187338250G>A , CM000666.1:g.187338250G>A	GRCh37
NC_000004.10:g.187575244G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033900.1:n.214+83749C>T
XR_427648.2:n.1186-760C>T
XR_939587.1:n.1354-760C>T
XR_939588.1:n.1074-760C>T
NR_033901.2:n.1573-760C>T