Canonical Allele Identifier: CA519355152

Gene: F8

Linked Data

• dbSNP Id: rs1210824418
• gnomAD v2: X-154065870-C-G
• gnomAD v3: X-154837595-C-G
• gnomAD v4: X-154837595-C-G
• MyVariant Identifiers: chrX:g.154065870C>G (hg19) ; chrX:g.154837595C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837595C>G , CM000685.2:g.154837595C>G	GRCh38
NC_000023.10:g.154065870C>G , CM000685.1:g.154065870C>G	GRCh37
NC_000023.9:g.153719064C>G	NCBI36
NG_011403.1:g.190129G>C
NG_033065.1:g.2068G>C
NG_011403.2:g.190129G>C

Transcript Alleles

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