Canonical Allele Identifier: CA343141961
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169541491G>T (hg19) chr1:g.169572253G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572253G>T , CM000663.2:g.169572253G>T GRCh38
NC_000001.10:g.169541491G>T , CM000663.1:g.169541491G>T GRCh37
NC_000001.9:g.167808115G>T NCBI36
NG_011806.1:g.19279C>A , LRG_553:g.19279C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.341C>A MANE Select ENSP00000356771.3:p.Pro114His
ENST00000367796.3:c.341C>A ENSP00000356770.3:p.Pro114His
ENST00000367797.7:c.341C>A ENSP00000356771.3:p.Pro114His
NM_000130.4:c.341C>A , LRG_553t1:c.341C>A NP_000121.2:p.Pro114His
XM_017000660.2:c.-71C>A XP_016856149.1:n.-71C>A
NM_000130.5:c.341C>A MANE Select NP_000121.2:p.Pro114His
Search 100 bp 5'
Search 100 bp 3'