Canonical Allele Identifier: CA645237050
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1557271022
MyVariant Identifiers: chrX:g.154065852A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837577A>G , CM000685.2:g.154837577A>G GRCh38
NC_000023.10:g.154065852A>G , CM000685.1:g.154065852A>G GRCh37
NC_000023.9:g.153719046A>G NCBI36
NG_011403.1:g.190147T>C
NG_033065.1:g.2086T>C
NG_011403.2:g.190147T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*20T>C MANE Select ENSP00000353393.4:n.*20T>C
ENST00000644698.1:c.*20T>C ENSP00000495706.1:n.*20T>C
ENST00000330287.10:c.*20T>C ENSP00000327895.6:n.*20T>C
ENST00000360256.8:c.*20T>C ENSP00000353393.4:n.*20T>C
NM_000132.3:c.*20T>C NP_000123.1:n.*20T>C
NM_019863.2:c.*20T>C NP_063916.1:n.*20T>C
XM_011531126.1:c.*20T>C XP_011529428.1:n.*20T>C
NM_000132.4:c.*20T>C MANE Select NP_000123.1:n.*20T>C
NM_019863.3:c.*20T>C NP_063916.1:n.*20T>C