Canonical Allele Identifier: CA118883977
Gene: MOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs113143621

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53098565A>G , CM000667.2:g.53098565A>G GRCh38
NC_000005.9:g.52394395A>G , CM000667.1:g.52394395A>G GRCh37
NC_000005.8:g.52430152A>G NCBI36
NG_008435.2:g.16204T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000396954.8:c.*37T>C MANE Select ENSP00000380157.3:n.*37T>C
ENST00000450852.8:c.*524T>C MANE Plus Clinical ENSP00000411022.3:n.*524T>C
ENST00000361377.8:c.*373T>C ENSP00000355160.4:n.*373T>C
ENST00000396954.7:c.*37T>C ENSP00000380157.3:n.*37T>C
ENST00000450852.7:c.*524T>C ENSP00000411022.3:n.*524T>C
ENST00000502402.5:n.2351T>C
ENST00000508922.5:c.*444T>C ENSP00000426274.1:n.*444T>C
ENST00000510818.6:c.*477T>C ENSP00000424267.2:n.*477T>C
ENST00000582677.5:c.*245T>C ENSP00000462870.1:n.*245T>C
ENST00000584946.5:c.*396T>C ENSP00000464663.1:n.*396T>C
NM_004531.4:c.*37T>C NP_004522.1:n.*37T>C
NM_176806.3:c.*524T>C NP_789776.1:n.*524T>C
NM_004531.5:c.*37T>C MANE Select NP_004522.1:n.*37T>C
NM_176806.4:c.*524T>C MANE Plus Clinical NP_789776.1:n.*524T>C