Canonical Allele Identifier: CA2695167351
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154837521-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837521C>T , CM000685.2:g.154837521C>T GRCh38
NC_000023.10:g.154065796C>T , CM000685.1:g.154065796C>T GRCh37
NC_000023.9:g.153718990C>T NCBI36
NG_011403.1:g.190203G>A
NG_033065.1:g.2142G>A
NG_011403.2:g.190203G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*76G>A MANE Select ENSP00000353393.4:n.*76G>A
ENST00000644698.1:c.*76G>A ENSP00000495706.1:n.*76G>A
ENST00000330287.10:c.*76G>A ENSP00000327895.6:n.*76G>A
ENST00000360256.8:c.*76G>A ENSP00000353393.4:n.*76G>A
NM_000132.3:c.*76G>A NP_000123.1:n.*76G>A
NM_019863.2:c.*76G>A NP_063916.1:n.*76G>A
XM_011531126.1:c.*76G>A XP_011529428.1:n.*76G>A
NM_000132.4:c.*76G>A MANE Select NP_000123.1:n.*76G>A
NM_019863.3:c.*76G>A NP_063916.1:n.*76G>A
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