Canonical Allele Identifier: CA1206156953
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1661108447

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169586503G>A , CM000663.2:g.169586503G>A GRCh38
NC_000001.10:g.169555741G>A , CM000663.1:g.169555741G>A GRCh37
NC_000001.9:g.167822365G>A NCBI36
NG_011806.1:g.5029C>T , LRG_553:g.5029C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367796.3:c.-117C>T ENSP00000356770.3:n.-117C>T
ENST00000367797.7:c.-117C>T ENSP00000356771.3:n.-117C>T
NM_000130.4:c.-117C>T , LRG_553t1:c.-117C>T NP_000121.2:n.-117C>T
XM_017000660.2:c.-436C>T XP_016856149.1:n.-436C>T