Canonical Allele Identifier: CA23513320

Gene: C1orf141

Linked Data

• dbSNP Id: rs889175826
• gnomAD v3: 1-67135359-T-G
• gnomAD v4: 1-67135359-T-G
• MyVariant Identifiers: chr1:g.67601042T>G (hg19) ; chr1:g.67135359T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67135359T>G , CM000663.2:g.67135359T>G	GRCh38
NC_000001.10:g.67601042T>G , CM000663.1:g.67601042T>G	GRCh37
NC_000001.9:g.67373630T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371007.6:c.-103-4132A>C	ENSP00000360046.1:n.-103-4132A>C
ENST00000448166.6:c.-103-4132A>C	ENSP00000415519.2:n.-103-4132A>C
XM_011541466.1:c.-18+6255A>C	XP_011539768.1:n.-18+6255A>C
XM_011541466.2:c.-18+6255A>C	XP_011539768.1:n.-18+6255A>C