Canonical Allele Identifier: CA2612565761
Gene: FAR1 HGNC NCBI

Linked Data

gnomAD v4: 11-13728580-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728580C>A , CM000673.2:g.13728580C>A GRCh38
NC_000011.9:g.13750127C>A , CM000673.1:g.13750127C>A GRCh37
NC_000011.8:g.13706703C>A NCBI36
NG_041826.1:g.64922C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*211-32C>A ENSP00000515269.1:n.*211-32C>A
ENST00000354817.8:c.1386-32C>A MANE Select ENSP00000346874.3:n.1386-32C>A
ENST00000354817.7:c.1386-32C>A ENSP00000346874.3:n.1386-32C>A
ENST00000532502.1:c.258-32C>A ENSP00000434624.1:n.258-32C>A
NM_032228.5:c.1386-32C>A NP_115604.1:n.1386-32C>A
XM_011520400.1:c.1395-32C>A XP_011518702.1:n.1395-32C>A
XM_011520401.1:c.1218-32C>A XP_011518703.1:n.1218-32C>A
XM_011520400.2:c.1395-32C>A XP_011518702.1:n.1395-32C>A
NM_032228.6:c.1386-32C>A MANE Select NP_115604.1:n.1386-32C>A
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