Canonical Allele Identifier: CA2649036271
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169555108-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555108T>C , CM000663.2:g.169555108T>C GRCh38
NC_000001.10:g.169524346T>C , CM000663.1:g.169524346T>C GRCh37
NC_000001.9:g.167790970T>C NCBI36
NG_011806.1:g.36424A>G , LRG_553:g.36424A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1118+74A>G MANE Select ENSP00000356771.3:n.1118+74A>G
ENST00000367796.3:c.1118+74A>G ENSP00000356770.3:n.1118+74A>G
ENST00000367797.7:c.1118+74A>G ENSP00000356771.3:n.1118+74A>G
NM_000130.4:c.1118+74A>G , LRG_553t1:c.1118+74A>G NP_000121.2:n.1118+74A>G
XM_017000660.2:c.707+74A>G XP_016856149.1:n.707+74A>G
NM_000130.5:c.1118+74A>G MANE Select NP_000121.2:n.1118+74A>G
Search 100 bp 5'
Search 100 bp 3'