Canonical Allele Identifier: CA935278879

Gene: FAR1

Linked Data

• dbSNP Id: rs1848689928
• gnomAD v3: 11-13728565-T-G
• gnomAD v4: 11-13728565-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728565T>G , CM000673.2:g.13728565T>G	GRCh38
NC_000011.9:g.13750112T>G , CM000673.1:g.13750112T>G	GRCh37
NC_000011.8:g.13706688T>G	NCBI36
NG_041826.1:g.64907T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703358.1:c.*211-47T>G	ENSP00000515269.1:n.*211-47T>G
ENST00000354817.8:c.1386-47T>G MANE Select	ENSP00000346874.3:n.1386-47T>G
ENST00000354817.7:c.1386-47T>G	ENSP00000346874.3:n.1386-47T>G
ENST00000532502.1:c.258-47T>G	ENSP00000434624.1:n.258-47T>G
NM_032228.5:c.1386-47T>G	NP_115604.1:n.1386-47T>G
XM_011520400.1:c.1395-47T>G	XP_011518702.1:n.1395-47T>G
XM_011520401.1:c.1218-47T>G	XP_011518703.1:n.1218-47T>G
XM_011520400.2:c.1395-47T>G	XP_011518702.1:n.1395-47T>G
NM_032228.6:c.1386-47T>G MANE Select	NP_115604.1:n.1386-47T>G