Canonical Allele Identifier: CA559320441

Gene: MOCS2

Linked Data

• dbSNP Id: rs1449196464
• gnomAD v2: 5-52394383-A-G
• gnomAD v4: 5-53098553-A-G
• MyVariant Identifiers: chr5:g.52394383A>G (hg19) ; chr5:g.53098553A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098553A>G , CM000667.2:g.53098553A>G	GRCh38
NC_000005.9:g.52394383A>G , CM000667.1:g.52394383A>G	GRCh37
NC_000005.8:g.52430140A>G	NCBI36
NG_008435.2:g.16216T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*49T>C MANE Select	ENSP00000380157.3:n.*49T>C
ENST00000450852.8:c.*536T>C MANE Plus Clinical	ENSP00000411022.3:n.*536T>C
ENST00000361377.8:c.*385T>C	ENSP00000355160.4:n.*385T>C
ENST00000396954.7:c.*49T>C	ENSP00000380157.3:n.*49T>C
ENST00000450852.7:c.*536T>C	ENSP00000411022.3:n.*536T>C
ENST00000502402.5:n.2363T>C
ENST00000508922.5:c.*456T>C	ENSP00000426274.1:n.*456T>C
ENST00000510818.6:c.*489T>C	ENSP00000424267.2:n.*489T>C
ENST00000582677.5:c.*257T>C	ENSP00000462870.1:n.*257T>C
ENST00000584946.5:c.*408T>C	ENSP00000464663.1:n.*408T>C
NM_004531.4:c.*49T>C	NP_004522.1:n.*49T>C
NM_176806.3:c.*536T>C	NP_789776.1:n.*536T>C
NM_004531.5:c.*49T>C MANE Select	NP_004522.1:n.*49T>C
NM_176806.4:c.*536T>C MANE Plus Clinical	NP_789776.1:n.*536T>C