Canonical Allele Identifier: CA572084105

Gene: C7orf50 CYP2W1

Linked Data

• dbSNP Id: rs1264196024
• gnomAD v2: 7-1022795-T-C
• gnomAD v4: 7-983159-T-C
• MyVariant Identifiers: chr7:g.1022795T>C (hg19) ; chr7:g.983159T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.983159T>C , CM000669.2:g.983159T>C	GRCh38
NC_000007.13:g.1022795T>C , CM000669.1:g.1022795T>C	GRCh37
NC_000007.12:g.989321T>C	NCBI36
NG_007934.1:g.4961T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_005249889.3:c.523-4098A>G (C7orf50)	XP_005249946.2:n.523-4098A>G
XM_011515440.1:c.-53T>C (CYP2W1)	XP_011513742.1:n.-53T>C
XM_011515441.1:c.-53T>C (CYP2W1)	XP_011513743.1:n.-53T>C
XM_011515580.1:c.1108-4098A>G (C7orf50)	XP_011513882.1:n.1108-4098A>G
XM_011515581.1:c.565-4098A>G (C7orf50)	XP_011513883.1:n.565-4098A>G
XM_011515582.1:c.565-4098A>G (C7orf50)	XP_011513884.1:n.565-4098A>G
XM_011515583.1:c.565-4098A>G (C7orf50)	XP_011513885.1:n.565-4098A>G
XM_011515584.1:c.565-4098A>G (C7orf50)	XP_011513886.1:n.565-4098A>G
NR_156697.1:n.548-4098A>G (C7orf50)
XM_011515440.3:c.-53T>C (CYP2W1)	XP_011513742.1:n.-53T>C
XM_011515441.3:c.-53T>C (CYP2W1)	XP_011513743.1:n.-53T>C
XM_011515581.3:c.565-4098A>G (C7orf50)	XP_011513883.1:n.565-4098A>G
XM_011515582.3:c.565-4098A>G (C7orf50)	XP_011513884.1:n.565-4098A>G
XM_011515583.2:c.565-4098A>G (C7orf50)	XP_011513885.1:n.565-4098A>G
XM_011515584.2:c.565-4098A>G (C7orf50)	XP_011513886.1:n.565-4098A>G
XM_017012720.2:c.565-4098A>G (C7orf50)	XP_016868209.1:n.565-4098A>G
XM_017012721.2:c.523-4098A>G (C7orf50)	XP_016868210.1:n.523-4098A>G
NR_156697.2:n.548-4098A>G (C7orf50)