Canonical Allele Identifier: CA2695170518
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-155022695-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022695T>G , CM000685.2:g.155022695T>G GRCh38
NC_000023.10:g.154250970T>G , CM000685.1:g.154250970T>G GRCh37
NC_000023.9:g.153904164T>G NCBI36
NG_011403.1:g.5029A>C
NG_011403.2:g.5029A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.-143A>C MANE Select ENSP00000353393.4:n.-143A>C
ENST00000647125.1:c.-143A>C ENSP00000496062.1:n.-143A>C
ENST00000360256.8:c.-143A>C ENSP00000353393.4:n.-143A>C
ENST00000423959.5:c.38+4085A>C ENSP00000409446.1:n.38+4085A>C
ENST00000453950.1:c.39-199A>C ENSP00000389153.1:n.39-199A>C
NM_000132.3:c.-143A>C NP_000123.1:n.-143A>C
XM_011531126.1:c.38+4085A>C XP_011529428.1:n.38+4085A>C
NM_000132.4:c.-143A>C MANE Select NP_000123.1:n.-143A>C
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