Canonical Allele Identifier: CA2579744059

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837799G>C , CM000685.2:g.154837799G>C	GRCh38
NC_000023.10:g.154066074G>C , CM000685.1:g.154066074G>C	GRCh37
NC_000023.9:g.153719268G>C	NCBI36
NG_011403.1:g.189925C>G
NG_033065.1:g.1864C>G
NG_011403.2:g.189925C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6901-47C>G MANE Select	ENSP00000353393.4:n.6901-47C>G
ENST00000644698.1:c.634-47C>G	ENSP00000495706.1:n.634-47C>G
ENST00000330287.10:c.496-47C>G	ENSP00000327895.6:n.496-47C>G
ENST00000360256.8:c.6901-47C>G	ENSP00000353393.4:n.6901-47C>G
NM_000132.3:c.6901-47C>G	NP_000123.1:n.6901-47C>G
NM_019863.2:c.496-47C>G	NP_063916.1:n.496-47C>G
XM_011531126.1:c.6796-47C>G	XP_011529428.1:n.6796-47C>G
NM_000132.4:c.6901-47C>G MANE Select	NP_000123.1:n.6901-47C>G
NM_019863.3:c.496-47C>G	NP_063916.1:n.496-47C>G