Canonical Allele Identifier: CA738098830

Gene: C1orf141

Linked Data

• dbSNP Id: rs1224623095
• gnomAD v3: 1-67135389-A-T
• gnomAD v4: 1-67135389-A-T
• MyVariant Identifiers: chr1:g.67601072A>T (hg19) ; chr1:g.67135389A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67135389A>T , CM000663.2:g.67135389A>T	GRCh38
NC_000001.10:g.67601072A>T , CM000663.1:g.67601072A>T	GRCh37
NC_000001.9:g.67373660A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371007.6:c.-103-4162T>A	ENSP00000360046.1:n.-103-4162T>A
ENST00000448166.6:c.-103-4162T>A	ENSP00000415519.2:n.-103-4162T>A
XM_011541466.1:c.-18+6225T>A	XP_011539768.1:n.-18+6225T>A
XM_011541466.2:c.-18+6225T>A	XP_011539768.1:n.-18+6225T>A