Canonical Allele Identifier: CA812031778

Gene: MOCS2

Linked Data

• dbSNP Id: rs1484034514
• MyVariant Identifiers: chr5:g.52394529A>G (hg19) ; chr5:g.53098699A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098699A>G , CM000667.2:g.53098699A>G	GRCh38
NC_000005.9:g.52394529A>G , CM000667.1:g.52394529A>G	GRCh37
NC_000005.8:g.52430286A>G	NCBI36
NG_008435.2:g.16070T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.502-32T>C MANE Select	ENSP00000380157.3:n.502-32T>C
ENST00000450852.8:c.*422-32T>C MANE Plus Clinical	ENSP00000411022.3:n.*422-32T>C
ENST00000361377.8:c.*271-32T>C	ENSP00000355160.4:n.*271-32T>C
ENST00000396954.7:c.502-32T>C	ENSP00000380157.3:n.502-32T>C
ENST00000450852.7:c.*422-32T>C	ENSP00000411022.3:n.*422-32T>C
ENST00000502402.5:n.2249-32T>C
ENST00000508922.5:c.*310T>C	ENSP00000426274.1:n.*310T>C
ENST00000510818.6:c.*375-32T>C	ENSP00000424267.2:n.*375-32T>C
ENST00000582677.5:c.*143-32T>C	ENSP00000462870.1:n.*143-32T>C
ENST00000584946.5:c.*294-32T>C	ENSP00000464663.1:n.*294-32T>C
NM_004531.4:c.502-32T>C	NP_004522.1:n.502-32T>C
NM_176806.3:c.*422-32T>C	NP_789776.1:n.*422-32T>C
NM_004531.5:c.502-32T>C MANE Select	NP_004522.1:n.502-32T>C
NM_176806.4:c.*422-32T>C MANE Plus Clinical	NP_789776.1:n.*422-32T>C