Canonical Allele Identifier: CA2466865459

Gene: F8

Linked Data

• dbSNP Id: rs1172699967

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022562C>G , CM000685.2:g.155022562C>G	GRCh38
NC_000023.10:g.154250837C>G , CM000685.1:g.154250837C>G	GRCh37
NC_000023.9:g.153904031C>G	NCBI36
NG_011403.1:g.5162G>C
NG_011403.2:g.5162G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-10G>C MANE Select	ENSP00000353393.4:n.-10G>C
ENST00000647125.1:c.-10G>C	ENSP00000496062.1:n.-10G>C
ENST00000360256.8:c.-10G>C	ENSP00000353393.4:n.-10G>C
ENST00000423959.5:c.38+4218G>C	ENSP00000409446.1:n.38+4218G>C
ENST00000453950.1:c.39-66G>C	ENSP00000389153.1:n.39-66G>C
NM_000132.3:c.-10G>C	NP_000123.1:n.-10G>C
XM_011531126.1:c.38+4218G>C	XP_011529428.1:n.38+4218G>C
NM_000132.4:c.-10G>C MANE Select	NP_000123.1:n.-10G>C