Canonical Allele Identifier: CA414906828
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863088A>G , CM000685.2:g.154863088A>G GRCh38
NC_000023.10:g.154091363A>G , CM000685.1:g.154091363A>G GRCh37
NC_000023.9:g.153744557A>G NCBI36
NG_011403.1:g.164636T>C
NG_011403.2:g.164636T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6569T>C MANE Select ENSP00000353393.4:p.Leu2190Ser
ENST00000644698.1:c.302T>C ENSP00000495706.1:p.Leu101Ser
ENST00000330287.10:c.164T>C ENSP00000327895.6:p.Leu55Ser
ENST00000360256.8:c.6569T>C ENSP00000353393.4:p.Leu2190Ser
NM_000132.3:c.6569T>C NP_000123.1:p.Leu2190Ser
NM_019863.2:c.164T>C NP_063916.1:p.Leu55Ser
XM_011531126.1:c.6464T>C XP_011529428.1:p.Leu2155Ser
NM_000132.4:c.6569T>C MANE Select NP_000123.1:p.Leu2190Ser
NM_019863.3:c.164T>C NP_063916.1:p.Leu55Ser