Canonical Allele Identifier: CA414906774

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091357C>G (hg19) ; chrX:g.154863082C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863082C>G , CM000685.2:g.154863082C>G	GRCh38
NC_000023.10:g.154091357C>G , CM000685.1:g.154091357C>G	GRCh37
NC_000023.9:g.153744551C>G	NCBI36
NG_011403.1:g.164642G>C
NG_011403.2:g.164642G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6574+1G>C MANE Select	ENSP00000353393.4:n.6574+1G>C
ENST00000644698.1:c.307+1G>C	ENSP00000495706.1:n.307+1G>C
ENST00000330287.10:c.169+1G>C	ENSP00000327895.6:n.169+1G>C
ENST00000360256.8:c.6574+1G>C	ENSP00000353393.4:n.6574+1G>C
NM_000132.3:c.6574+1G>C	NP_000123.1:n.6574+1G>C
NM_019863.2:c.169+1G>C	NP_063916.1:n.169+1G>C
XM_011531126.1:c.6469+1G>C	XP_011529428.1:n.6469+1G>C
NM_000132.4:c.6574+1G>C MANE Select	NP_000123.1:n.6574+1G>C
NM_019863.3:c.169+1G>C	NP_063916.1:n.169+1G>C