Canonical Allele Identifier: CA414907252
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863131T>C , CM000685.2:g.154863131T>C GRCh38
NC_000023.10:g.154091406T>C , CM000685.1:g.154091406T>C GRCh37
NC_000023.9:g.153744600T>C NCBI36
NG_011403.1:g.164593A>G
NG_011403.2:g.164593A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6526A>G MANE Select ENSP00000353393.4:p.Ser2176Gly
ENST00000644698.1:c.259A>G ENSP00000495706.1:p.Ser87Gly
ENST00000330287.10:c.121A>G ENSP00000327895.6:p.Ser41Gly
ENST00000360256.8:c.6526A>G ENSP00000353393.4:p.Ser2176Gly
NM_000132.3:c.6526A>G NP_000123.1:p.Ser2176Gly
NM_019863.2:c.121A>G NP_063916.1:p.Ser41Gly
XM_011531126.1:c.6421A>G XP_011529428.1:p.Ser2141Gly
NM_000132.4:c.6526A>G MANE Select NP_000123.1:p.Ser2176Gly
NM_019863.3:c.121A>G NP_063916.1:p.Ser41Gly