Canonical Allele Identifier: CA564905546

Gene: MSX2

Linked Data

• dbSNP Id: rs1399837339
• gnomAD v2: 5-174151568-G-T
• gnomAD v3: 5-174724565-G-T
• gnomAD v4: 5-174724565-G-T
• MyVariant Identifiers: chr5:g.174151568G>T (hg19) ; chr5:g.174724565G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724565G>T , CM000667.2:g.174724565G>T	GRCh38
NC_000005.9:g.174151568G>T , CM000667.1:g.174151568G>T	GRCh37
NC_000005.8:g.174084174G>T	NCBI36
NG_008124.1:g.4994G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.6:c.-95G>T	ENSP00000239243.5:n.-95G>T