Canonical Allele Identifier: CA2649034530
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169526021-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169526021A>G , CM000663.2:g.169526021A>G GRCh38
NC_000001.10:g.169495259A>G , CM000663.1:g.169495259A>G GRCh37
NC_000001.9:g.167761883A>G NCBI36
NG_011806.1:g.65511T>C , LRG_553:g.65511T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.5600-4T>C MANE Select ENSP00000356771.3:n.5600-4T>C
ENST00000367796.3:c.5615-4T>C ENSP00000356770.3:n.5615-4T>C
ENST00000367797.7:c.5600-4T>C ENSP00000356771.3:n.5600-4T>C
NM_000130.4:c.5600-4T>C , LRG_553t1:c.5600-4T>C NP_000121.2:n.5600-4T>C
XM_017000660.2:c.5189-4T>C XP_016856149.1:n.5189-4T>C
NM_000130.5:c.5600-4T>C MANE Select NP_000121.2:n.5600-4T>C
Search 100 bp 5'
Search 100 bp 3'