Canonical Allele Identifier: CA526713589
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1190675395
gnomAD v2: 1-169541417-T-G
gnomAD v4: 1-169572179-T-G
MyVariant Identifiers: chr1:g.169541417T>G (hg19) chr1:g.169572179T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572179T>G , CM000663.2:g.169572179T>G GRCh38
NC_000001.10:g.169541417T>G , CM000663.1:g.169541417T>G GRCh37
NC_000001.9:g.167808041T>G NCBI36
NG_011806.1:g.19353A>C , LRG_553:g.19353A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.373+42A>C MANE Select ENSP00000356771.3:n.373+42A>C
ENST00000367796.3:c.373+42A>C ENSP00000356770.3:n.373+42A>C
ENST00000367797.7:c.373+42A>C ENSP00000356771.3:n.373+42A>C
NM_000130.4:c.373+42A>C , LRG_553t1:c.373+42A>C NP_000121.2:n.373+42A>C
XM_017000660.2:c.-39+42A>C XP_016856149.1:n.-39+42A>C
NM_000130.5:c.373+42A>C MANE Select NP_000121.2:n.373+42A>C
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