Canonical Allele Identifier: CA356137472
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737875457
gnomAD v3: 4-4860152-G-A
gnomAD v4: 4-4860152-G-A
MyVariant Identifiers: chr4:g.4861879G>A (hg19) chr4:g.4860152G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860152G>A , CM000666.2:g.4860152G>A GRCh38
NC_000004.11:g.4861879G>A , CM000666.1:g.4861879G>A GRCh37
NC_000004.10:g.4912780G>A NCBI36
NG_008121.1:g.5488G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.253G>A MANE Select ENSP00000372170.4:p.Gly85Ser
ENST00000382723.4:c.253G>A ENSP00000372170.4:p.Gly85Ser
NM_002448.3:c.253G>A MANE Select NP_002439.2:p.Gly85Ser
Search 100 bp 5'
Search 100 bp 3'