Canonical Allele Identifier: CA414897938
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837751A>C , CM000685.2:g.154837751A>C GRCh38
NC_000023.10:g.154066026A>C , CM000685.1:g.154066026A>C GRCh37
NC_000023.9:g.153719220A>C NCBI36
NG_011403.1:g.189973T>G
NG_033065.1:g.1912T>G
NG_011403.2:g.189973T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6902T>G MANE Select ENSP00000353393.4:p.Val2301Gly
ENST00000644698.1:c.635T>G ENSP00000495706.1:p.Val212Gly
ENST00000330287.10:c.497T>G ENSP00000327895.6:p.Val166Gly
ENST00000360256.8:c.6902T>G ENSP00000353393.4:p.Val2301Gly
NM_000132.3:c.6902T>G NP_000123.1:p.Val2301Gly
NM_019863.2:c.497T>G NP_063916.1:p.Val166Gly
XM_011531126.1:c.6797T>G XP_011529428.1:p.Val2266Gly
NM_000132.4:c.6902T>G MANE Select NP_000123.1:p.Val2301Gly
NM_019863.3:c.497T>G NP_063916.1:p.Val166Gly