Canonical Allele Identifier: CA1233914
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs778723822
ExAC: 1:169510907 T / A
gnomAD v2: 1-169510907-T-A
gnomAD v4: 1-169541669-T-A
MyVariant Identifiers: chr1:g.169510907T>A (hg19) chr1:g.169541669T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541669T>A , CM000663.2:g.169541669T>A GRCh38
NC_000001.10:g.169510907T>A , CM000663.1:g.169510907T>A GRCh37
NC_000001.9:g.167777531T>A NCBI36
NG_011806.1:g.49863A>T , LRG_553:g.49863A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.3421A>T MANE Select ENSP00000356771.3:p.Thr1141Ser
ENST00000367796.3:c.3436A>T ENSP00000356770.3:p.Thr1146Ser
ENST00000367797.7:c.3421A>T ENSP00000356771.3:p.Thr1141Ser
NM_000130.4:c.3421A>T , LRG_553t1:c.3421A>T NP_000121.2:p.Thr1141Ser
XM_017000660.2:c.3010A>T XP_016856149.1:p.Thr1004Ser
NM_000130.5:c.3421A>T MANE Select NP_000121.2:p.Thr1141Ser
Search 100 bp 5'
Search 100 bp 3'