Canonical Allele Identifier: CA414911642
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956974C>T , CM000685.2:g.154956974C>T GRCh38
NC_000023.10:g.154185249C>T , CM000685.1:g.154185249C>T GRCh37
NC_000023.9:g.153838443C>T NCBI36
NG_011403.1:g.70750G>A
NG_011403.2:g.70750G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1735G>A MANE Select ENSP00000353393.4:p.Asp579Asn
ENST00000647125.1:c.*1611G>A ENSP00000496062.1:n.*1611G>A
ENST00000360256.8:c.1735G>A ENSP00000353393.4:p.Asp579Asn
NM_000132.3:c.1735G>A NP_000123.1:p.Asp579Asn
XM_011531126.1:c.1630G>A XP_011529428.1:p.Asp544Asn
NM_000132.4:c.1735G>A MANE Select NP_000123.1:p.Asp579Asn