Canonical Allele Identifier: CA2602720024
Gene: F8 HGNC NCBI

Linked Data

gnomAD v3: X-154956893-C-G
gnomAD v4: X-154956893-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956893C>G , CM000685.2:g.154956893C>G GRCh38
NC_000023.10:g.154185168C>G , CM000685.1:g.154185168C>G GRCh37
NC_000023.9:g.153838362C>G NCBI36
NG_011403.1:g.70831G>C
NG_011403.2:g.70831G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1752+64G>C MANE Select ENSP00000353393.4:n.1752+64G>C
ENST00000647125.1:c.*1628+64G>C ENSP00000496062.1:n.*1628+64G>C
ENST00000360256.8:c.1752+64G>C ENSP00000353393.4:n.1752+64G>C
NM_000132.3:c.1752+64G>C NP_000123.1:n.1752+64G>C
XM_011531126.1:c.1647+64G>C XP_011529428.1:n.1647+64G>C
NM_000132.4:c.1752+64G>C MANE Select NP_000123.1:n.1752+64G>C
Search 100 bp 5'
Search 100 bp 3'