Canonical Allele Identifier: CA11138836
Gene: FARSB HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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