Canonical Allele Identifier: CA218132524
Gene: FAR1 HGNC NCBI

Linked Data

dbSNP Id: rs768727620
gnomAD v4: 11-13728571-T-C
MyVariant Identifiers: chr11:g.13750118T>C (hg19) chr11:g.13728571T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728571T>C , CM000673.2:g.13728571T>C GRCh38
NC_000011.9:g.13750118T>C , CM000673.1:g.13750118T>C GRCh37
NC_000011.8:g.13706694T>C NCBI36
NG_041826.1:g.64913T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703358.1:c.*211-41T>C ENSP00000515269.1:n.*211-41T>C
ENST00000354817.8:c.1386-41T>C MANE Select ENSP00000346874.3:n.1386-41T>C
ENST00000354817.7:c.1386-41T>C ENSP00000346874.3:n.1386-41T>C
ENST00000532502.1:c.258-41T>C ENSP00000434624.1:n.258-41T>C
NM_032228.5:c.1386-41T>C NP_115604.1:n.1386-41T>C
XM_011520400.1:c.1395-41T>C XP_011518702.1:n.1395-41T>C
XM_011520401.1:c.1218-41T>C XP_011518703.1:n.1218-41T>C
XM_011520400.2:c.1395-41T>C XP_011518702.1:n.1395-41T>C
NM_032228.6:c.1386-41T>C MANE Select NP_115604.1:n.1386-41T>C
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