Canonical Allele Identifier: CA765279869

Gene: FARSB

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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