Canonical Allele Identifier: CA2695167329
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837484G>A , CM000685.2:g.154837484G>A GRCh38
NC_000023.10:g.154065759G>A , CM000685.1:g.154065759G>A GRCh37
NC_000023.9:g.153718953G>A NCBI36
NG_011403.1:g.190240C>T
NG_033065.1:g.2179C>T
NG_011403.2:g.190240C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*113C>T MANE Select ENSP00000353393.4:n.*113C>T
ENST00000644698.1:c.*113C>T ENSP00000495706.1:n.*113C>T
ENST00000330287.10:c.*113C>T ENSP00000327895.6:n.*113C>T
ENST00000360256.8:c.*113C>T ENSP00000353393.4:n.*113C>T
NM_000132.3:c.*113C>T NP_000123.1:n.*113C>T
NM_019863.2:c.*113C>T NP_063916.1:n.*113C>T
XM_011531126.1:c.*113C>T XP_011529428.1:n.*113C>T
NM_000132.4:c.*113C>T MANE Select NP_000123.1:n.*113C>T
NM_019863.3:c.*113C>T NP_063916.1:n.*113C>T