Canonical Allele Identifier: CA2613835813
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392290-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392290C>T , CM000673.2:g.61392290C>T GRCh38
NC_000011.9:g.61159762C>T , CM000673.1:g.61159762C>T GRCh37
NC_000011.8:g.60916338C>T NCBI36
NG_032976.1:g.4931C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-342C>T ENSP00000440638.1:n.-342C>T
XM_005274039.3:c.-673C>T XP_005274096.1:n.-673C>T
XM_005274039.4:c.-673C>T XP_005274096.1:n.-673C>T
Search 100 bp 5'
Search 100 bp 3'