Canonical Allele Identifier: CA414896782
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837634A>G , CM000685.2:g.154837634A>G GRCh38
NC_000023.10:g.154065909A>G , CM000685.1:g.154065909A>G GRCh37
NC_000023.9:g.153719103A>G NCBI36
NG_011403.1:g.190090T>C
NG_033065.1:g.2029T>C
NG_011403.2:g.190090T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.7019T>C MANE Select ENSP00000353393.4:p.Met2340Thr
ENST00000644698.1:c.752T>C ENSP00000495706.1:p.Met251Thr
ENST00000330287.10:c.614T>C ENSP00000327895.6:p.Met205Thr
ENST00000360256.8:c.7019T>C ENSP00000353393.4:p.Met2340Thr
NM_000132.3:c.7019T>C NP_000123.1:p.Met2340Thr
NM_019863.2:c.614T>C NP_063916.1:p.Met205Thr
XM_011531126.1:c.6914T>C XP_011529428.1:p.Met2305Thr
NM_000132.4:c.7019T>C MANE Select NP_000123.1:p.Met2340Thr
NM_019863.3:c.614T>C NP_063916.1:p.Met205Thr