Canonical Allele Identifier: CA414907315
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863136T>G , CM000685.2:g.154863136T>G GRCh38
NC_000023.10:g.154091411T>G , CM000685.1:g.154091411T>G GRCh37
NC_000023.9:g.153744605T>G NCBI36
NG_011403.1:g.164588A>C
NG_011403.2:g.164588A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6521A>C MANE Select ENSP00000353393.4:p.His2174Pro
ENST00000644698.1:c.254A>C ENSP00000495706.1:p.His85Pro
ENST00000330287.10:c.116A>C ENSP00000327895.6:p.His39Pro
ENST00000360256.8:c.6521A>C ENSP00000353393.4:p.His2174Pro
NM_000132.3:c.6521A>C NP_000123.1:p.His2174Pro
NM_019863.2:c.116A>C NP_063916.1:p.His39Pro
XM_011531126.1:c.6416A>C XP_011529428.1:p.His2139Pro
NM_000132.4:c.6521A>C MANE Select NP_000123.1:p.His2174Pro
NM_019863.3:c.116A>C NP_063916.1:p.His39Pro