Canonical Allele Identifier: CA1138595142

Gene: F8

Linked Data

• dbSNP Id: rs2072482978
• gnomAD v3: X-154837516-GA-G
• gnomAD v4: X-154837516-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837518del , CM000685.2:g.154837518del	GRCh38
NC_000023.10:g.154065793del , CM000685.1:g.154065793del	GRCh37
NC_000023.9:g.153718987del	NCBI36
NG_011403.1:g.190207del
NG_033065.1:g.2146del
NG_011403.2:g.190207del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*80del MANE Select	ENSP00000353393.4:n.*80del
ENST00000644698.1:c.*80del	ENSP00000495706.1:n.*80del
ENST00000330287.10:c.*80del	ENSP00000327895.6:n.*80del
ENST00000360256.8:c.*80del	ENSP00000353393.4:n.*80del
NM_000132.3:c.*80del	NP_000123.1:n.*80del
NM_019863.2:c.*80del	NP_063916.1:n.*80del
XM_011531126.1:c.*80del	XP_011529428.1:n.*80del
NM_000132.4:c.*80del MANE Select	NP_000123.1:n.*80del
NM_019863.3:c.*80del	NP_063916.1:n.*80del