Canonical Allele Identifier: CA1138595131

Gene: F8

Linked Data

• dbSNP Id: rs2072481922
• gnomAD v3: X-154837416-G-A
• gnomAD v4: X-154837416-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837416G>A , CM000685.2:g.154837416G>A	GRCh38
NC_000023.10:g.154065691G>A , CM000685.1:g.154065691G>A	GRCh37
NC_000023.9:g.153718885G>A	NCBI36
NG_011403.1:g.190308C>T
NG_033065.1:g.2247C>T
NG_011403.2:g.190308C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.*181C>T MANE Select	ENSP00000353393.4:n.*181C>T
ENST00000644698.1:c.*181C>T	ENSP00000495706.1:n.*181C>T
ENST00000330287.10:c.*181C>T	ENSP00000327895.6:n.*181C>T
ENST00000360256.8:c.*181C>T	ENSP00000353393.4:n.*181C>T
NM_000132.3:c.*181C>T	NP_000123.1:n.*181C>T
NM_019863.2:c.*181C>T	NP_063916.1:n.*181C>T
XM_011531126.1:c.*181C>T	XP_011529428.1:n.*181C>T
NM_000132.4:c.*181C>T MANE Select	NP_000123.1:n.*181C>T
NM_019863.3:c.*181C>T	NP_063916.1:n.*181C>T