Canonical Allele Identifier: CA332650424

Gene: CHM

Linked Data

• dbSNP Id: rs747006109
• gnomAD v2: X-85155634-T-C
• gnomAD v4: X-85900629-T-C
• MyVariant Identifiers: chrX:g.85155634T>C (hg19) ; chrX:g.85900629T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85900629T>C , CM000685.2:g.85900629T>C	GRCh38
NC_000023.10:g.85155634T>C , CM000685.1:g.85155634T>C	GRCh37
NC_000023.9:g.85042290T>C	NCBI36
NG_009874.2:g.151934A>G , LRG_699:g.151934A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000357749.7:c.1413+17A>G MANE Select	ENSP00000350386.2:n.1413+17A>G
ENST00000357749.6:c.1413+17A>G	ENSP00000350386.2:n.1413+17A>G
ENST00000467744.2:n.127-37535A>G
NM_000390.2:c.1413+17A>G , LRG_699t1:c.1413+17A>G	NP_000381.1:n.1413+17A>G
XM_006724615.2:c.1350+17A>G	XP_006724678.1:n.1350+17A>G
XM_011530839.1:c.969+17A>G	XP_011529141.1:n.969+17A>G
NM_000390.3:c.1413+17A>G	NP_000381.1:n.1413+17A>G
NM_001320959.1:c.969+17A>G	NP_001307888.1:n.969+17A>G
NM_001362517.1:c.969+17A>G	NP_001349446.1:n.969+17A>G
NM_001362518.1:c.969+17A>G	NP_001349447.1:n.969+17A>G
NM_001362519.1:c.969+17A>G	NP_001349448.1:n.969+17A>G
XM_017029242.2:c.1413+17A>G	XP_016884731.1:n.1413+17A>G
XM_017029246.1:c.969+17A>G	XP_016884735.1:n.969+17A>G
XM_024452331.1:c.969+17A>G	XP_024308099.1:n.969+17A>G
NM_000390.4:c.1413+17A>G MANE Select	NP_000381.1:n.1413+17A>G
NM_001362518.2:c.969+17A>G	NP_001349447.1:n.969+17A>G