Canonical Allele Identifier: CA343146278
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169510360G>C (hg19) chr1:g.169541122G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541122G>C , CM000663.2:g.169541122G>C GRCh38
NC_000001.10:g.169510360G>C , CM000663.1:g.169510360G>C GRCh37
NC_000001.9:g.167776984G>C NCBI36
NG_011806.1:g.50410C>G , LRG_553:g.50410C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.3968C>G MANE Select ENSP00000356771.3:p.Pro1323Arg
ENST00000367796.3:c.3983C>G ENSP00000356770.3:p.Pro1328Arg
ENST00000367797.7:c.3968C>G ENSP00000356771.3:p.Pro1323Arg
NM_000130.4:c.3968C>G , LRG_553t1:c.3968C>G NP_000121.2:p.Pro1323Arg
XM_017000660.2:c.3557C>G XP_016856149.1:p.Pro1186Arg
NM_000130.5:c.3968C>G MANE Select NP_000121.2:p.Pro1323Arg
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