Canonical Allele Identifier: CA1602344877
Gene: MSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1581516125
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724566C>G , CM000667.2:g.174724566C>G GRCh38
NC_000005.9:g.174151569C>G , CM000667.1:g.174151569C>G GRCh37
NC_000005.8:g.174084175C>G NCBI36
NG_008124.1:g.4995C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-94C>G ENSP00000239243.5:n.-94C>G
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