Canonical Allele Identifier: CA414904286
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860545T>A , CM000685.2:g.154860545T>A GRCh38
NC_000023.10:g.154088820T>A , CM000685.1:g.154088820T>A GRCh37
NC_000023.9:g.153742014T>A NCBI36
NG_011403.1:g.167179A>T
NG_011403.2:g.167179A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6787A>T MANE Select ENSP00000353393.4:p.Thr2263Ser
ENST00000644698.1:c.520A>T ENSP00000495706.1:p.Thr174Ser
ENST00000330287.10:c.382A>T ENSP00000327895.6:p.Thr128Ser
ENST00000360256.8:c.6787A>T ENSP00000353393.4:p.Thr2263Ser
NM_000132.3:c.6787A>T NP_000123.1:p.Thr2263Ser
NM_019863.2:c.382A>T NP_063916.1:p.Thr128Ser
XM_011531126.1:c.6682A>T XP_011529428.1:p.Thr2228Ser
NM_000132.4:c.6787A>T MANE Select NP_000123.1:p.Thr2263Ser
NM_019863.3:c.382A>T NP_063916.1:p.Thr128Ser