Canonical Allele Identifier: CA2695167327
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154837477-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837477G>T , CM000685.2:g.154837477G>T GRCh38
NC_000023.10:g.154065752G>T , CM000685.1:g.154065752G>T GRCh37
NC_000023.9:g.153718946G>T NCBI36
NG_011403.1:g.190247C>A
NG_033065.1:g.2186C>A
NG_011403.2:g.190247C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*120C>A MANE Select ENSP00000353393.4:n.*120C>A
ENST00000644698.1:c.*120C>A ENSP00000495706.1:n.*120C>A
ENST00000330287.10:c.*120C>A ENSP00000327895.6:n.*120C>A
ENST00000360256.8:c.*120C>A ENSP00000353393.4:n.*120C>A
NM_000132.3:c.*120C>A NP_000123.1:n.*120C>A
NM_019863.2:c.*120C>A NP_063916.1:n.*120C>A
XM_011531126.1:c.*120C>A XP_011529428.1:n.*120C>A
NM_000132.4:c.*120C>A MANE Select NP_000123.1:n.*120C>A
NM_019863.3:c.*120C>A NP_063916.1:n.*120C>A
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