Canonical Allele Identifier: CA1206148887
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1660750705
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572572G>A , CM000663.2:g.169572572G>A GRCh38
NC_000001.10:g.169541810G>A , CM000663.1:g.169541810G>A GRCh37
NC_000001.9:g.167808434G>A NCBI36
NG_011806.1:g.18960C>T , LRG_553:g.18960C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-229C>T MANE Select ENSP00000356771.3:n.251-229C>T
ENST00000367796.3:c.251-229C>T ENSP00000356770.3:n.251-229C>T
ENST00000367797.7:c.251-229C>T ENSP00000356771.3:n.251-229C>T
NM_000130.4:c.251-229C>T , LRG_553t1:c.251-229C>T NP_000121.2:n.251-229C>T
XM_017000660.2:c.-161-229C>T XP_016856149.1:n.-161-229C>T
NM_000130.5:c.251-229C>T MANE Select NP_000121.2:n.251-229C>T
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