Canonical Allele Identifier: CA414907898
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2072707185

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863205G>A , CM000685.2:g.154863205G>A GRCh38
NC_000023.10:g.154091480G>A , CM000685.1:g.154091480G>A GRCh37
NC_000023.9:g.153744674G>A NCBI36
NG_011403.1:g.164519C>T
NG_011403.2:g.164519C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6452C>T MANE Select ENSP00000353393.4:p.Ser2151Leu
ENST00000644698.1:c.185C>T ENSP00000495706.1:p.Ser62Leu
ENST00000330287.10:c.47C>T ENSP00000327895.6:p.Ser16Leu
ENST00000360256.8:c.6452C>T ENSP00000353393.4:p.Ser2151Leu
NM_000132.3:c.6452C>T NP_000123.1:p.Ser2151Leu
NM_019863.2:c.47C>T NP_063916.1:p.Ser16Leu
XM_011531126.1:c.6347C>T XP_011529428.1:p.Ser2116Leu
NM_000132.4:c.6452C>T MANE Select NP_000123.1:p.Ser2151Leu
NM_019863.3:c.47C>T NP_063916.1:p.Ser16Leu