Canonical Allele Identifier: CA343130703

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169498984T>C (hg19) ; chr1:g.169529746T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529746T>C , CM000663.2:g.169529746T>C	GRCh38
NC_000001.10:g.169498984T>C , CM000663.1:g.169498984T>C	GRCh37
NC_000001.9:g.167765608T>C	NCBI36
NG_011806.1:g.61786A>G , LRG_553:g.61786A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367797.9:c.5281A>G MANE Select	ENSP00000356771.3:p.Asn1761Asp
ENST00000367796.3:c.5296A>G	ENSP00000356770.3:p.Asn1766Asp
ENST00000367797.7:c.5281A>G	ENSP00000356771.3:p.Asn1761Asp
NM_000130.4:c.5281A>G , LRG_553t1:c.5281A>G	NP_000121.2:p.Asn1761Asp
XM_017000660.2:c.4870A>G	XP_016856149.1:p.Asn1624Asp
NM_000130.5:c.5281A>G MANE Select	NP_000121.2:p.Asn1761Asp