Canonical Allele Identifier: CA343130999
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169524448C>G (hg19) chr1:g.169555210C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555210C>G , CM000663.2:g.169555210C>G GRCh38
NC_000001.10:g.169524448C>G , CM000663.1:g.169524448C>G GRCh37
NC_000001.9:g.167791072C>G NCBI36
NG_011806.1:g.36322G>C , LRG_553:g.36322G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.1090G>C MANE Select ENSP00000356771.3:p.Ala364Pro
ENST00000367796.3:c.1090G>C ENSP00000356770.3:p.Ala364Pro
ENST00000367797.7:c.1090G>C ENSP00000356771.3:p.Ala364Pro
NM_000130.4:c.1090G>C , LRG_553t1:c.1090G>C NP_000121.2:p.Ala364Pro
XM_017000660.2:c.679G>C XP_016856149.1:p.Ala227Pro
NM_000130.5:c.1090G>C MANE Select NP_000121.2:p.Ala364Pro
Search 100 bp 5'
Search 100 bp 3'