Canonical Allele Identifier: CA2574085079
Gene: F5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169529568G>C , CM000663.2:g.169529568G>C GRCh38
NC_000001.10:g.169498806G>C , CM000663.1:g.169498806G>C GRCh37
NC_000001.9:g.167765430G>C NCBI36
NG_011806.1:g.61964C>G , LRG_553:g.61964C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5419+40C>G MANE Select ENSP00000356771.3:n.5419+40C>G
ENST00000367796.3:c.5434+40C>G ENSP00000356770.3:n.5434+40C>G
ENST00000367797.7:c.5419+40C>G ENSP00000356771.3:n.5419+40C>G
NM_000130.4:c.5419+40C>G , LRG_553t1:c.5419+40C>G NP_000121.2:n.5419+40C>G
XM_017000660.2:c.5008+40C>G XP_016856149.1:n.5008+40C>G
NM_000130.5:c.5419+40C>G MANE Select NP_000121.2:n.5419+40C>G
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