Canonical Allele Identifier: CA447978531
Gene: MSX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.174151908G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724905G>C , CM000667.2:g.174724905G>C GRCh38
NC_000005.9:g.174151908G>C , CM000667.1:g.174151908G>C GRCh37
NC_000005.8:g.174084514G>C NCBI36
NG_008124.1:g.5334G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000239243.7:c.246G>C MANE Select ENSP00000239243.5:p.Ser82=
ENST00000239243.6:c.246G>C ENSP00000239243.5:p.Ser82=
ENST00000507785.2:c.246G>C ENSP00000427425.1:p.Ser82=
NM_002449.4:c.246G>C NP_002440.2:p.Ser82=
NM_001363626.1:c.246G>C NP_001350555.1:p.Ser82=
NM_002449.5:c.246G>C MANE Select NP_002440.2:p.Ser82=
NM_001363626.2:c.246G>C NP_001350555.1:p.Ser82=
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