Canonical Allele Identifier: CA1233915
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs745472773
ExAC: 1:169510920 A / G
gnomAD v2: 1-169510920-A-G
gnomAD v4: 1-169541682-A-G
MyVariant Identifiers: chr1:g.169510920A>G (hg19) chr1:g.169541682A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541682A>G , CM000663.2:g.169541682A>G GRCh38
NC_000001.10:g.169510920A>G , CM000663.1:g.169510920A>G GRCh37
NC_000001.9:g.167777544A>G NCBI36
NG_011806.1:g.49850T>C , LRG_553:g.49850T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.3408T>C MANE Select ENSP00000356771.3:p.Asp1136=
ENST00000367796.3:c.3423T>C ENSP00000356770.3:p.Asp1141=
ENST00000367797.7:c.3408T>C ENSP00000356771.3:p.Asp1136=
NM_000130.4:c.3408T>C , LRG_553t1:c.3408T>C NP_000121.2:p.Asp1136=
XM_017000660.2:c.2997T>C XP_016856149.1:p.Asp999=
NM_000130.5:c.3408T>C MANE Select NP_000121.2:p.Asp1136=
Search 100 bp 5'
Search 100 bp 3'