Canonical Allele Identifier: CA2612565755
Gene: FAR1 HGNC NCBI

Linked Data

gnomAD v4: 11-13728573-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728573G>C , CM000673.2:g.13728573G>C GRCh38
NC_000011.9:g.13750120G>C , CM000673.1:g.13750120G>C GRCh37
NC_000011.8:g.13706696G>C NCBI36
NG_041826.1:g.64915G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*211-39G>C ENSP00000515269.1:n.*211-39G>C
ENST00000354817.8:c.1386-39G>C MANE Select ENSP00000346874.3:n.1386-39G>C
ENST00000354817.7:c.1386-39G>C ENSP00000346874.3:n.1386-39G>C
ENST00000532502.1:c.258-39G>C ENSP00000434624.1:n.258-39G>C
NM_032228.5:c.1386-39G>C NP_115604.1:n.1386-39G>C
XM_011520400.1:c.1395-39G>C XP_011518702.1:n.1395-39G>C
XM_011520401.1:c.1218-39G>C XP_011518703.1:n.1218-39G>C
XM_011520400.2:c.1395-39G>C XP_011518702.1:n.1395-39G>C
NM_032228.6:c.1386-39G>C MANE Select NP_115604.1:n.1386-39G>C
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