Canonical Allele Identifier: CA2739149230

Gene: F8

Linked Data

• dbSNP Id: rs2123995502

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903491A>C , CM000685.2:g.154903491A>C	GRCh38
NC_000023.10:g.154131766A>C , CM000685.1:g.154131766A>C	GRCh37
NC_000023.9:g.153784960A>C	NCBI36
NG_011403.1:g.124233T>G
NG_011403.2:g.124233T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5998+415T>G MANE Select	ENSP00000353393.4:n.5998+415T>G
ENST00000360256.8:c.5998+415T>G	ENSP00000353393.4:n.5998+415T>G
NM_000132.3:c.5998+415T>G	NP_000123.1:n.5998+415T>G
XM_011531126.1:c.5893+415T>G	XP_011529428.1:n.5893+415T>G
NM_000132.4:c.5998+415T>G MANE Select	NP_000123.1:n.5998+415T>G