Canonical Allele Identifier: CA414897183
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837679A>T , CM000685.2:g.154837679A>T GRCh38
NC_000023.10:g.154065954A>T , CM000685.1:g.154065954A>T GRCh37
NC_000023.9:g.153719148A>T NCBI36
NG_011403.1:g.190045T>A
NG_033065.1:g.1984T>A
NG_011403.2:g.190045T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6974T>A MANE Select ENSP00000353393.4:p.Leu2325His
ENST00000644698.1:c.707T>A ENSP00000495706.1:p.Leu236His
ENST00000330287.10:c.569T>A ENSP00000327895.6:p.Leu190His
ENST00000360256.8:c.6974T>A ENSP00000353393.4:p.Leu2325His
NM_000132.3:c.6974T>A NP_000123.1:p.Leu2325His
NM_019863.2:c.569T>A NP_063916.1:p.Leu190His
XM_011531126.1:c.6869T>A XP_011529428.1:p.Leu2290His
NM_000132.4:c.6974T>A MANE Select NP_000123.1:p.Leu2325His
NM_019863.3:c.569T>A NP_063916.1:p.Leu190His