Canonical Allele Identifier: CA414907018
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863105C>G , CM000685.2:g.154863105C>G GRCh38
NC_000023.10:g.154091380C>G , CM000685.1:g.154091380C>G GRCh37
NC_000023.9:g.153744574C>G NCBI36
NG_011403.1:g.164619G>C
NG_011403.2:g.164619G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6552G>C MANE Select ENSP00000353393.4:p.Glu2184Asp
ENST00000644698.1:c.285G>C ENSP00000495706.1:p.Glu95Asp
ENST00000330287.10:c.147G>C ENSP00000327895.6:p.Glu49Asp
ENST00000360256.8:c.6552G>C ENSP00000353393.4:p.Glu2184Asp
NM_000132.3:c.6552G>C NP_000123.1:p.Glu2184Asp
NM_019863.2:c.147G>C NP_063916.1:p.Glu49Asp
XM_011531126.1:c.6447G>C XP_011529428.1:p.Glu2149Asp
NM_000132.4:c.6552G>C MANE Select NP_000123.1:p.Glu2184Asp
NM_019863.3:c.147G>C NP_063916.1:p.Glu49Asp