Canonical Allele Identifier: CA23513313

Gene: C1orf141

Linked Data

• dbSNP Id: rs148643208
• MyVariant Identifiers: chr1:g.67601036T>C (hg19) ; chr1:g.67135353T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67135353T>C , CM000663.2:g.67135353T>C	GRCh38
NC_000001.10:g.67601036T>C , CM000663.1:g.67601036T>C	GRCh37
NC_000001.9:g.67373624T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000371007.6:c.-103-4126A>G	ENSP00000360046.1:n.-103-4126A>G
ENST00000448166.6:c.-103-4126A>G	ENSP00000415519.2:n.-103-4126A>G
XM_011541466.1:c.-18+6261A>G	XP_011539768.1:n.-18+6261A>G
XM_011541466.2:c.-18+6261A>G	XP_011539768.1:n.-18+6261A>G