Canonical Allele Identifier: CA2466857814
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073622057

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997111G>A , CM000685.2:g.154997111G>A GRCh38
NC_000023.10:g.154225386G>A , CM000685.1:g.154225386G>A GRCh37
NC_000023.9:g.153878580G>A NCBI36
NG_011403.1:g.30613C>T
NG_011403.2:g.30613C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.266-16C>T MANE Select ENSP00000353393.4:n.266-16C>T
ENST00000647125.1:c.*52-16C>T ENSP00000496062.1:n.*52-16C>T
ENST00000360256.8:c.266-16C>T ENSP00000353393.4:n.266-16C>T
ENST00000423959.5:c.161-16C>T ENSP00000409446.1:n.161-16C>T
ENST00000453950.1:c.248-16C>T ENSP00000389153.1:n.248-16C>T
NM_000132.3:c.266-16C>T NP_000123.1:n.266-16C>T
XM_011531126.1:c.161-16C>T XP_011529428.1:n.161-16C>T
NM_000132.4:c.266-16C>T MANE Select NP_000123.1:n.266-16C>T