Canonical Allele Identifier: CA559320442

Gene: MOCS2

Linked Data

• dbSNP Id: rs1434013451
• gnomAD v2: 5-52394408-T-C
• gnomAD v4: 5-53098578-T-C
• MyVariant Identifiers: chr5:g.52394408T>C (hg19) ; chr5:g.53098578T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098578T>C , CM000667.2:g.53098578T>C	GRCh38
NC_000005.9:g.52394408T>C , CM000667.1:g.52394408T>C	GRCh37
NC_000005.8:g.52430165T>C	NCBI36
NG_008435.2:g.16191A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.*24A>G MANE Select	ENSP00000380157.3:n.*24A>G
ENST00000450852.8:c.*511A>G MANE Plus Clinical	ENSP00000411022.3:n.*511A>G
ENST00000361377.8:c.*360A>G	ENSP00000355160.4:n.*360A>G
ENST00000396954.7:c.*24A>G	ENSP00000380157.3:n.*24A>G
ENST00000450852.7:c.*511A>G	ENSP00000411022.3:n.*511A>G
ENST00000502402.5:n.2338A>G
ENST00000508922.5:c.*431A>G	ENSP00000426274.1:n.*431A>G
ENST00000510818.6:c.*464A>G	ENSP00000424267.2:n.*464A>G
ENST00000582677.5:c.*232A>G	ENSP00000462870.1:n.*232A>G
ENST00000584946.5:c.*383A>G	ENSP00000464663.1:n.*383A>G
NM_004531.4:c.*24A>G	NP_004522.1:n.*24A>G
NM_176806.3:c.*511A>G	NP_789776.1:n.*511A>G
NM_004531.5:c.*24A>G MANE Select	NP_004522.1:n.*24A>G
NM_176806.4:c.*511A>G MANE Plus Clinical	NP_789776.1:n.*511A>G