Canonical Allele Identifier: CA343124939
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169495198G>C (hg19) chr1:g.169525960G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169525960G>C , CM000663.2:g.169525960G>C GRCh38
NC_000001.10:g.169495198G>C , CM000663.1:g.169495198G>C GRCh37
NC_000001.9:g.167761822G>C NCBI36
NG_011806.1:g.65572C>G , LRG_553:g.65572C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5657C>G MANE Select ENSP00000356771.3:p.Thr1886Arg
ENST00000367796.3:c.5672C>G ENSP00000356770.3:p.Thr1891Arg
ENST00000367797.7:c.5657C>G ENSP00000356771.3:p.Thr1886Arg
NM_000130.4:c.5657C>G , LRG_553t1:c.5657C>G NP_000121.2:p.Thr1886Arg
XM_017000660.2:c.5246C>G XP_016856149.1:p.Thr1749Arg
NM_000130.5:c.5657C>G MANE Select NP_000121.2:p.Thr1886Arg
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