Canonical Allele Identifier: CA519355274
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154065968T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837693T>C , CM000685.2:g.154837693T>C GRCh38
NC_000023.10:g.154065968T>C , CM000685.1:g.154065968T>C GRCh37
NC_000023.9:g.153719162T>C NCBI36
NG_011403.1:g.190031A>G
NG_033065.1:g.1970A>G
NG_011403.2:g.190031A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6960A>G MANE Select ENSP00000353393.4:p.Leu2320=
ENST00000644698.1:c.693A>G ENSP00000495706.1:p.Leu231=
ENST00000330287.10:c.555A>G ENSP00000327895.6:p.Leu185=
ENST00000360256.8:c.6960A>G ENSP00000353393.4:p.Leu2320=
NM_000132.3:c.6960A>G NP_000123.1:p.Leu2320=
NM_019863.2:c.555A>G NP_063916.1:p.Leu185=
XM_011531126.1:c.6855A>G XP_011529428.1:p.Leu2285=
NM_000132.4:c.6960A>G MANE Select NP_000123.1:p.Leu2320=
NM_019863.3:c.555A>G NP_063916.1:p.Leu185=