Canonical Allele Identifier: CA414905995
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903989A>C , CM000685.2:g.154903989A>C GRCh38
NC_000023.10:g.154132264A>C , CM000685.1:g.154132264A>C GRCh37
NC_000023.9:g.153785458A>C NCBI36
NG_011403.1:g.123735T>G
NG_011403.2:g.123735T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5915T>G MANE Select ENSP00000353393.4:p.Ile1972Ser
ENST00000360256.8:c.5915T>G ENSP00000353393.4:p.Ile1972Ser
NM_000132.3:c.5915T>G NP_000123.1:p.Ile1972Ser
XM_011531126.1:c.5810T>G XP_011529428.1:p.Ile1937Ser
NM_000132.4:c.5915T>G MANE Select NP_000123.1:p.Ile1972Ser