Canonical Allele Identifier: CA350815693

Gene: FARSB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222613892T>G , CM000664.2:g.222613892T>G	GRCh38
NC_000002.11:g.223478611T>G , CM000664.1:g.223478611T>G	GRCh37
NC_000002.10:g.223186855T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005687.5:c.1381A>C MANE Select	NP_005678.3:p.Thr461Pro
ENST00000281828.8:c.1381A>C MANE Select	ENSP00000281828.6:p.Thr461Pro
NM_005687.4:c.1381A>C	NP_005678.3:p.Thr461Pro
NR_130154.1:n.1859A>C
NR_130154.2:n.1596A>C
ENST00000281828.6:c.1381A>C	ENSP00000281828.6:p.Thr461Pro
XM_006712169.1:c.1084A>C	XP_006712232.1:p.Thr362Pro
XM_006712169.2:c.1084A>C	XP_006712232.1:p.Thr362Pro
XM_006712170.1:c.1084A>C	XP_006712233.1:p.Thr362Pro
XM_011510466.1:c.1084A>C	XP_011508768.1:p.Thr362Pro
XM_011510466.2:c.1084A>C	XP_011508768.1:p.Thr362Pro
XM_017003110.2:c.1084A>C	XP_016858599.1:p.Thr362Pro
XM_024452492.1:c.1084A>C	XP_024308260.1:p.Thr362Pro