Canonical Allele Identifier: CA414906039
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073023517

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903993T>G , CM000685.2:g.154903993T>G GRCh38
NC_000023.10:g.154132268T>G , CM000685.1:g.154132268T>G GRCh37
NC_000023.9:g.153785462T>G NCBI36
NG_011403.1:g.123731A>C
NG_011403.2:g.123731A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5911A>C MANE Select ENSP00000353393.4:p.Asn1971His
ENST00000360256.8:c.5911A>C ENSP00000353393.4:p.Asn1971His
NM_000132.3:c.5911A>C NP_000123.1:p.Asn1971His
XM_011531126.1:c.5806A>C XP_011529428.1:p.Asn1936His
NM_000132.4:c.5911A>C MANE Select NP_000123.1:p.Asn1971His