Canonical Allele Identifier: CA438366321
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4863005-C-G
MyVariant Identifiers: chr4:g.4864732C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863005C>G , CM000666.2:g.4863005C>G GRCh38
NC_000004.11:g.4864732C>G , CM000666.1:g.4864732C>G GRCh37
NC_000004.10:g.4915633C>G NCBI36
NG_008121.1:g.8341C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.774C>G MANE Select ENSP00000372170.4:p.Gly258=
ENST00000382723.4:c.774C>G ENSP00000372170.4:p.Gly258=
ENST00000468421.1:n.486C>G
NM_002448.3:c.774C>G MANE Select NP_002439.2:p.Gly258=
Search 100 bp 5'
Search 100 bp 3'