Canonical Allele Identifier: CA2676572710

Gene: MSX2

Linked Data

• gnomAD v4: 5-174724630-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724630G>T , CM000667.2:g.174724630G>T	GRCh38
NC_000005.9:g.174151633G>T , CM000667.1:g.174151633G>T	GRCh37
NC_000005.8:g.174084239G>T	NCBI36
NG_008124.1:g.5059G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.-30G>T MANE Select	ENSP00000239243.5:n.-30G>T
ENST00000239243.6:c.-30G>T	ENSP00000239243.5:n.-30G>T
ENST00000507785.2:c.-30G>T	ENSP00000427425.1:n.-30G>T
NM_002449.4:c.-30G>T	NP_002440.2:n.-30G>T
NM_001363626.1:c.-30G>T	NP_001350555.1:n.-30G>T
NM_002449.5:c.-30G>T MANE Select	NP_002440.2:n.-30G>T
NM_001363626.2:c.-30G>T	NP_001350555.1:n.-30G>T