Canonical Allele Identifier: CA2578521472
Gene: FARS2 HGNC NCBI

Linked Data

gnomAD v4: 6-5369181-A-AG

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.5369183dup , CM000668.2:g.5369183dup GRCh38
NC_000006.11:g.5369416dup , CM000668.1:g.5369416dup GRCh37
NC_000006.10:g.5314415dup NCBI36
NG_033003.1:g.112833dup
NG_033003.2:g.112833dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000274680.9:c.612+1dup
ENST00000648580.1:c.612+1dup
ENST00000274680.8:c.612+1dup
ENST00000324331.10:c.612+1dup
NM_006567.3:c.612+1dup
XM_005248811.1:c.612+1dup
XM_005248812.2:c.612+1dup
XM_006714966.1:c.612+1dup
XM_011514247.1:c.612+1dup
XM_011514248.1:c.612+1dup
XM_011514249.1:c.612+1dup
XM_011514250.1:c.612+1dup
XM_011514251.1:c.612+1dup
XR_926026.1:n.943+1dup
XR_926027.1:n.943+1dup
XR_926028.1:n.943+1dup
NM_001318872.1:c.612+1dup
NM_006567.4:c.612+1dup
XM_005248812.3:c.612+1dup
XM_006714966.3:c.612+1dup
XM_011514247.3:c.612+1dup
XM_011514248.3:c.612+1dup
XM_011514249.2:c.612+1dup
XM_011514251.3:c.612+1dup
XM_017010186.1:c.612+1dup
XM_017010187.1:c.612+1dup
XR_926027.3:n.920+1dup
XR_926028.2:n.920+1dup
NM_001318872.2:c.612+1dup
NM_001374875.1:c.612+1dup
NM_001374876.1:c.612+1dup
NM_001374877.1:c.612+1dup
NM_001374878.1:c.612+1dup
NM_001374879.1:c.612+1dup
NM_001375257.1:c.612+1dup
NM_001375258.1:c.612+1dup
NM_001375259.1:c.-84-35359dup NP_001362188.1:n.-84-35359dup
NM_001375260.1:c.-340-27450dup NP_001362189.1:n.-340-27450dup
NM_006567.5:c.612+1dup