Canonical Allele Identifier: CA658572073
Gene: F8 HGNC NCBI

Linked Data

COSMIC: COSN6494565
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022584G>T , CM000685.2:g.155022584G>T GRCh38
NC_000023.10:g.154250859G>T , CM000685.1:g.154250859G>T GRCh37
NC_000023.9:g.153904053G>T NCBI36
NG_011403.1:g.5140C>A
NG_011403.2:g.5140C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.-32C>A MANE Select ENSP00000353393.4:n.-32C>A
ENST00000647125.1:c.-32C>A ENSP00000496062.1:n.-32C>A
ENST00000360256.8:c.-32C>A ENSP00000353393.4:n.-32C>A
ENST00000423959.5:c.38+4196C>A ENSP00000409446.1:n.38+4196C>A
ENST00000453950.1:c.39-88C>A ENSP00000389153.1:n.39-88C>A
NM_000132.3:c.-32C>A NP_000123.1:n.-32C>A
XM_011531126.1:c.38+4196C>A XP_011529428.1:n.38+4196C>A
NM_000132.4:c.-32C>A MANE Select NP_000123.1:n.-32C>A
Search 100 bp 5'
Search 100 bp 3'