Canonical Allele Identifier: CA414905974
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903984A>G , CM000685.2:g.154903984A>G GRCh38
NC_000023.10:g.154132259A>G , CM000685.1:g.154132259A>G GRCh37
NC_000023.9:g.153785453A>G NCBI36
NG_011403.1:g.123740T>C
NG_011403.2:g.123740T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5920T>C MANE Select ENSP00000353393.4:p.Ser1974Pro
ENST00000360256.8:c.5920T>C ENSP00000353393.4:p.Ser1974Pro
NM_000132.3:c.5920T>C NP_000123.1:p.Ser1974Pro
XM_011531126.1:c.5815T>C XP_011529428.1:p.Ser1939Pro
NM_000132.4:c.5920T>C MANE Select NP_000123.1:p.Ser1974Pro