Canonical Allele Identifier: CA414907538
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863158A>C , CM000685.2:g.154863158A>C GRCh38
NC_000023.10:g.154091433A>C , CM000685.1:g.154091433A>C GRCh37
NC_000023.9:g.153744627A>C NCBI36
NG_011403.1:g.164566T>G
NG_011403.2:g.164566T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6499T>G MANE Select ENSP00000353393.4:p.Tyr2167Asp
ENST00000644698.1:c.232T>G ENSP00000495706.1:p.Tyr78Asp
ENST00000330287.10:c.94T>G ENSP00000327895.6:p.Tyr32Asp
ENST00000360256.8:c.6499T>G ENSP00000353393.4:p.Tyr2167Asp
NM_000132.3:c.6499T>G NP_000123.1:p.Tyr2167Asp
NM_019863.2:c.94T>G NP_063916.1:p.Tyr32Asp
XM_011531126.1:c.6394T>G XP_011529428.1:p.Tyr2132Asp
NM_000132.4:c.6499T>G MANE Select NP_000123.1:p.Tyr2167Asp
NM_019863.3:c.94T>G NP_063916.1:p.Tyr32Asp