Canonical Allele Identifier: CA2676572649
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724567-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724567G>C , CM000667.2:g.174724567G>C GRCh38
NC_000005.9:g.174151570G>C , CM000667.1:g.174151570G>C GRCh37
NC_000005.8:g.174084176G>C NCBI36
NG_008124.1:g.4996G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.6:c.-93G>C ENSP00000239243.5:n.-93G>C
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