Canonical Allele Identifier: CA1330704921

Gene: FARSB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.222652986C= , CM000664.2:g.222652986C=	GRCh38
NC_000002.11:g.223517705C= , CM000664.1:g.223517705C=	GRCh37
NC_000002.10:g.223225949C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005687.5:c.58+3030G= MANE Select	NP_005678.3:n.58+3030G=
ENST00000281828.8:c.58+3030G= MANE Select	ENSP00000281828.6:n.58+3030G=
NM_005687.4:c.58+3030G=	NP_005678.3:n.58+3030G=
NR_130154.1:n.340+3030G=
NR_130154.2:n.77+3030G=
ENST00000281828.6:c.58+3030G=	ENSP00000281828.6:n.58+3030G=
XM_006712169.1:c.-410+3030G=	XP_006712232.1:n.-410+3030G=
XM_006712169.2:c.-410+3030G=	XP_006712232.1:n.-410+3030G=
XM_006712170.1:c.-765+3030G=	XP_006712233.1:n.-765+3030G=
XM_011510466.1:c.-277+3030G=	XP_011508768.1:n.-277+3030G=
XM_011510466.2:c.-277+3030G=	XP_011508768.1:n.-277+3030G=
XM_017003110.2:c.-2681+3030G=	XP_016858599.1:n.-2681+3030G=
XM_024452492.1:c.-765+3030G=	XP_024308260.1:n.-765+3030G=