Canonical Allele Identifier: CA2695168757
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154928433-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928433C>G , CM000685.2:g.154928433C>G GRCh38
NC_000023.10:g.154156708C>G , CM000685.1:g.154156708C>G GRCh37
NC_000023.9:g.153809902C>G NCBI36
NG_011403.1:g.99291G>C
NG_011403.2:g.99291G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+138G>C MANE Select ENSP00000353393.4:n.5219+138G>C
ENST00000360256.8:c.5219+138G>C ENSP00000353393.4:n.5219+138G>C
NM_000132.3:c.5219+138G>C NP_000123.1:n.5219+138G>C
XM_011531126.1:c.5114+138G>C XP_011529428.1:n.5114+138G>C
NM_000132.4:c.5219+138G>C MANE Select NP_000123.1:n.5219+138G>C
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