Canonical Allele Identifier: CA414897585
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837722G>C , CM000685.2:g.154837722G>C GRCh38
NC_000023.10:g.154065997G>C , CM000685.1:g.154065997G>C GRCh37
NC_000023.9:g.153719191G>C NCBI36
NG_011403.1:g.190002C>G
NG_033065.1:g.1941C>G
NG_011403.2:g.190002C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6931C>G MANE Select ENSP00000353393.4:p.Pro2311Ala
ENST00000644698.1:c.664C>G ENSP00000495706.1:p.Pro222Ala
ENST00000330287.10:c.526C>G ENSP00000327895.6:p.Pro176Ala
ENST00000360256.8:c.6931C>G ENSP00000353393.4:p.Pro2311Ala
NM_000132.3:c.6931C>G NP_000123.1:p.Pro2311Ala
NM_019863.2:c.526C>G NP_063916.1:p.Pro176Ala
XM_011531126.1:c.6826C>G XP_011529428.1:p.Pro2276Ala
NM_000132.4:c.6931C>G MANE Select NP_000123.1:p.Pro2311Ala
NM_019863.3:c.526C>G NP_063916.1:p.Pro176Ala