Canonical Allele Identifier: CA414907525
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863157T>G , CM000685.2:g.154863157T>G GRCh38
NC_000023.10:g.154091432T>G , CM000685.1:g.154091432T>G GRCh37
NC_000023.9:g.153744626T>G NCBI36
NG_011403.1:g.164567A>C
NG_011403.2:g.164567A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6500A>C MANE Select ENSP00000353393.4:p.Tyr2167Ser
ENST00000644698.1:c.233A>C ENSP00000495706.1:p.Tyr78Ser
ENST00000330287.10:c.95A>C ENSP00000327895.6:p.Tyr32Ser
ENST00000360256.8:c.6500A>C ENSP00000353393.4:p.Tyr2167Ser
NM_000132.3:c.6500A>C NP_000123.1:p.Tyr2167Ser
NM_019863.2:c.95A>C NP_063916.1:p.Tyr32Ser
XM_011531126.1:c.6395A>C XP_011529428.1:p.Tyr2132Ser
NM_000132.4:c.6500A>C MANE Select NP_000123.1:p.Tyr2167Ser
NM_019863.3:c.95A>C NP_063916.1:p.Tyr32Ser