Canonical Allele Identifier: CA890938642
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1174909892
MyVariant Identifiers: chr1:g.169541776T>G (hg19) chr1:g.169572538T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572538T>G , CM000663.2:g.169572538T>G GRCh38
NC_000001.10:g.169541776T>G , CM000663.1:g.169541776T>G GRCh37
NC_000001.9:g.167808400T>G NCBI36
NG_011806.1:g.18994A>C , LRG_553:g.18994A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-195A>C MANE Select ENSP00000356771.3:n.251-195A>C
ENST00000367796.3:c.251-195A>C ENSP00000356770.3:n.251-195A>C
ENST00000367797.7:c.251-195A>C ENSP00000356771.3:n.251-195A>C
NM_000130.4:c.251-195A>C , LRG_553t1:c.251-195A>C NP_000121.2:n.251-195A>C
XM_017000660.2:c.-161-195A>C XP_016856149.1:n.-161-195A>C
NM_000130.5:c.251-195A>C MANE Select NP_000121.2:n.251-195A>C
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