Canonical Allele Identifier: CA890928759
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1399597500
MyVariant Identifiers: chr1:g.169522099T>C (hg19) chr1:g.169552861T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552861T>C , CM000663.2:g.169552861T>C GRCh38
NC_000001.10:g.169522099T>C , CM000663.1:g.169522099T>C GRCh37
NC_000001.9:g.167788723T>C NCBI36
NG_011806.1:g.38671A>G , LRG_553:g.38671A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1119-127A>G MANE Select ENSP00000356771.3:n.1119-127A>G
ENST00000367796.3:c.1119-127A>G ENSP00000356770.3:n.1119-127A>G
ENST00000367797.7:c.1119-127A>G ENSP00000356771.3:n.1119-127A>G
NM_000130.4:c.1119-127A>G , LRG_553t1:c.1119-127A>G NP_000121.2:n.1119-127A>G
XM_017000660.2:c.708-127A>G XP_016856149.1:n.708-127A>G
NM_000130.5:c.1119-127A>G MANE Select NP_000121.2:n.1119-127A>G
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