Canonical Allele Identifier: CA343130659
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169498983T>G (hg19) chr1:g.169529745T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169529745T>G , CM000663.2:g.169529745T>G GRCh38
NC_000001.10:g.169498983T>G , CM000663.1:g.169498983T>G GRCh37
NC_000001.9:g.167765607T>G NCBI36
NG_011806.1:g.61787A>C , LRG_553:g.61787A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5282A>C MANE Select ENSP00000356771.3:p.Asn1761Thr
ENST00000367796.3:c.5297A>C ENSP00000356770.3:p.Asn1766Thr
ENST00000367797.7:c.5282A>C ENSP00000356771.3:p.Asn1761Thr
NM_000130.4:c.5282A>C , LRG_553t1:c.5282A>C NP_000121.2:p.Asn1761Thr
XM_017000660.2:c.4871A>C XP_016856149.1:p.Asn1624Thr
NM_000130.5:c.5282A>C MANE Select NP_000121.2:p.Asn1761Thr
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