Canonical Allele Identifier: CA10465556

Gene: CHM

Linked Data

• ClinVar Variation Id: 796016
• ClinVar RCV Id: RCV000979375 ; RCV001832267
• dbSNP Id: rs374880482
• ExAC: X:85218753 T / C
• gnomAD v2: X-85218753-T-C
• gnomAD v3: X-85963748-T-C
• gnomAD v4: X-85963748-T-C
• MyVariant Identifiers: chrX:g.85218753T>C (hg19) ; chrX:g.85963748T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.85963748T>C , CM000685.2:g.85963748T>C	GRCh38
NC_000023.10:g.85218753T>C , CM000685.1:g.85218753T>C	GRCh37
NC_000023.9:g.85105409T>C	NCBI36
NG_009874.2:g.88815A>G , LRG_699:g.88815A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357749.7:c.619A>G MANE Select	ENSP00000350386.2:p.Thr207Ala
ENST00000357749.6:c.619A>G	ENSP00000350386.2:p.Thr207Ala
ENST00000467744.2:n.126+63743A>G
NM_000390.2:c.619A>G , LRG_699t1:c.619A>G	NP_000381.1:p.Thr207Ala
XM_006724615.2:c.556A>G	XP_006724678.1:p.Thr186Ala
XM_011530839.1:c.175A>G	XP_011529141.1:p.Thr59Ala
NM_000390.3:c.619A>G	NP_000381.1:p.Thr207Ala
NM_001320959.1:c.175A>G	NP_001307888.1:p.Thr59Ala
NM_001362517.1:c.175A>G	NP_001349446.1:p.Thr59Ala
NM_001362518.1:c.175A>G	NP_001349447.1:p.Thr59Ala
NM_001362519.1:c.175A>G	NP_001349448.1:p.Thr59Ala
XM_017029242.2:c.619A>G	XP_016884731.1:p.Thr207Ala
XM_017029246.1:c.175A>G	XP_016884735.1:p.Thr59Ala
XM_024452331.1:c.175A>G	XP_024308099.1:p.Thr59Ala
NM_000390.4:c.619A>G MANE Select	NP_000381.1:p.Thr207Ala
NM_001362518.2:c.175A>G	NP_001349447.1:p.Thr59Ala