Canonical Allele Identifier: CA873360674
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1372600816
MyVariant Identifiers: chrX:g.154837411A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837411A>T , CM000685.2:g.154837411A>T GRCh38
NC_000023.10:g.154065686A>T , CM000685.1:g.154065686A>T GRCh37
NC_000023.9:g.153718880A>T NCBI36
NG_011403.1:g.190313T>A
NG_033065.1:g.2252T>A
NG_011403.2:g.190313T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.*186T>A MANE Select ENSP00000353393.4:n.*186T>A
ENST00000644698.1:c.*186T>A ENSP00000495706.1:n.*186T>A
ENST00000330287.10:c.*186T>A ENSP00000327895.6:n.*186T>A
ENST00000360256.8:c.*186T>A ENSP00000353393.4:n.*186T>A
NM_000132.3:c.*186T>A NP_000123.1:n.*186T>A
NM_019863.2:c.*186T>A NP_063916.1:n.*186T>A
XM_011531126.1:c.*186T>A XP_011529428.1:n.*186T>A
NM_000132.4:c.*186T>A MANE Select NP_000123.1:n.*186T>A
NM_019863.3:c.*186T>A NP_063916.1:n.*186T>A
Search 100 bp 5'
Search 100 bp 3'