Canonical Allele Identifier: CA414907300
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863135A>C , CM000685.2:g.154863135A>C GRCh38
NC_000023.10:g.154091410A>C , CM000685.1:g.154091410A>C GRCh37
NC_000023.9:g.153744604A>C NCBI36
NG_011403.1:g.164589T>G
NG_011403.2:g.164589T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6522T>G MANE Select ENSP00000353393.4:p.His2174Gln
ENST00000644698.1:c.255T>G ENSP00000495706.1:p.His85Gln
ENST00000330287.10:c.117T>G ENSP00000327895.6:p.His39Gln
ENST00000360256.8:c.6522T>G ENSP00000353393.4:p.His2174Gln
NM_000132.3:c.6522T>G NP_000123.1:p.His2174Gln
NM_019863.2:c.117T>G NP_063916.1:p.His39Gln
XM_011531126.1:c.6417T>G XP_011529428.1:p.His2139Gln
NM_000132.4:c.6522T>G MANE Select NP_000123.1:p.His2174Gln
NM_019863.3:c.117T>G NP_063916.1:p.His39Gln