Canonical Allele Identifier: CA2669788600
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4863168-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863168G>T , CM000666.2:g.4863168G>T GRCh38
NC_000004.11:g.4864895G>T , CM000666.1:g.4864895G>T GRCh37
NC_000004.10:g.4915796G>T NCBI36
NG_008121.1:g.8504G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*25G>T MANE Select ENSP00000372170.4:n.*25G>T
ENST00000382723.4:c.*25G>T ENSP00000372170.4:n.*25G>T
NM_002448.3:c.*25G>T MANE Select NP_002439.2:n.*25G>T
Search 100 bp 5'
Search 100 bp 3'