Canonical Allele Identifier: CA32406014
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs995550281
gnomAD v2: 1-169541835-T-C
gnomAD v3: 1-169572597-T-C
gnomAD v4: 1-169572597-T-C
MyVariant Identifiers: chr1:g.169541835T>C (hg19) chr1:g.169572597T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572597T>C , CM000663.2:g.169572597T>C GRCh38
NC_000001.10:g.169541835T>C , CM000663.1:g.169541835T>C GRCh37
NC_000001.9:g.167808459T>C NCBI36
NG_011806.1:g.18935A>G , LRG_553:g.18935A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-254A>G MANE Select ENSP00000356771.3:n.251-254A>G
ENST00000367796.3:c.251-254A>G ENSP00000356770.3:n.251-254A>G
ENST00000367797.7:c.251-254A>G ENSP00000356771.3:n.251-254A>G
NM_000130.4:c.251-254A>G , LRG_553t1:c.251-254A>G NP_000121.2:n.251-254A>G
XM_017000660.2:c.-161-254A>G XP_016856149.1:n.-161-254A>G
NM_000130.5:c.251-254A>G MANE Select NP_000121.2:n.251-254A>G
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