Canonical Allele Identifier: CA11798629

Gene: F11-AS1

Linked Data

• dbSNP Id: rs11935103
• gnomAD v2: 4-187338335-C-T
• gnomAD v3: 4-186417181-C-T
• gnomAD v4: 4-186417181-C-T
• MyVariant Identifiers: chr4:g.187338335C>T (hg19) ; chr4:g.186417181C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186417181C>T , CM000666.2:g.186417181C>T	GRCh38
NC_000004.11:g.187338335C>T , CM000666.1:g.187338335C>T	GRCh37
NC_000004.10:g.187575329C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_033900.1:n.214+83664G>A
XR_427648.2:n.1186-845G>A
XR_939587.1:n.1354-845G>A
XR_939588.1:n.1074-845G>A
NR_033901.2:n.1573-845G>A