Canonical Allele Identifier: CA15100274
Gene: C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs114370420
gnomAD v2: 1-67601084-G-A
gnomAD v3: 1-67135401-G-A
gnomAD v4: 1-67135401-G-A
MyVariant Identifiers: chr1:g.67601084G>A (hg19) chr1:g.67135401G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67135401G>A , CM000663.2:g.67135401G>A GRCh38
NC_000001.10:g.67601084G>A , CM000663.1:g.67601084G>A GRCh37
NC_000001.9:g.67373672G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000371007.6:c.-103-4174C>T ENSP00000360046.1:n.-103-4174C>T
ENST00000448166.6:c.-103-4174C>T ENSP00000415519.2:n.-103-4174C>T
XM_011541466.1:c.-18+6213C>T XP_011539768.1:n.-18+6213C>T
XM_011541466.2:c.-18+6213C>T XP_011539768.1:n.-18+6213C>T
Search 100 bp 5'
Search 100 bp 3'