Canonical Allele Identifier: CA2649035877
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169530746-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169530746G>A , CM000663.2:g.169530746G>A GRCh38
NC_000001.10:g.169499984G>A , CM000663.1:g.169499984G>A GRCh37
NC_000001.9:g.167766608G>A NCBI36
NG_011806.1:g.60786C>T , LRG_553:g.60786C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5208+40C>T MANE Select ENSP00000356771.3:n.5208+40C>T
ENST00000367796.3:c.5223+40C>T ENSP00000356770.3:n.5223+40C>T
ENST00000367797.7:c.5208+40C>T ENSP00000356771.3:n.5208+40C>T
NM_000130.4:c.5208+40C>T , LRG_553t1:c.5208+40C>T NP_000121.2:n.5208+40C>T
XM_017000660.2:c.4797+40C>T XP_016856149.1:n.4797+40C>T
NM_000130.5:c.5208+40C>T MANE Select NP_000121.2:n.5208+40C>T
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