Canonical Allele Identifier: CA519352984
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154124490T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896215T>A , CM000685.2:g.154896215T>A GRCh38
NC_000023.10:g.154124490T>A , CM000685.1:g.154124490T>A GRCh37
NC_000023.9:g.153777684T>A NCBI36
NG_011403.1:g.131509A>T
NG_011403.2:g.131509A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6291A>T MANE Select ENSP00000353393.4:p.Pro2097=
ENST00000360256.8:c.6291A>T ENSP00000353393.4:p.Pro2097=
NM_000132.3:c.6291A>T NP_000123.1:p.Pro2097=
XM_011531126.1:c.6186A>T XP_011529428.1:p.Pro2062=
NM_000132.4:c.6291A>T MANE Select NP_000123.1:p.Pro2097=
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