Canonical Allele Identifier: CA362229581

Gene: MSX2

Linked Data

• dbSNP Id: rs1760750603
• MyVariant Identifiers: chr5:g.174151991A>C (hg19) ; chr5:g.174724988A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724988A>C , CM000667.2:g.174724988A>C	GRCh38
NC_000005.9:g.174151991A>C , CM000667.1:g.174151991A>C	GRCh37
NC_000005.8:g.174084597A>C	NCBI36
NG_008124.1:g.5417A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.329A>C MANE Select	ENSP00000239243.5:p.Glu110Ala
ENST00000239243.6:c.329A>C	ENSP00000239243.5:p.Glu110Ala
ENST00000507785.2:c.329A>C	ENSP00000427425.1:p.Glu110Ala
NM_002449.4:c.329A>C	NP_002440.2:p.Glu110Ala
NM_001363626.1:c.329A>C	NP_001350555.1:p.Glu110Ala
NM_002449.5:c.329A>C MANE Select	NP_002440.2:p.Glu110Ala
NM_001363626.2:c.329A>C	NP_001350555.1:p.Glu110Ala