Canonical Allele Identifier: CA2613835831
Gene: TMEM216 HGNC NCBI

Linked Data

gnomAD v4: 11-61392311-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392311G>T , CM000673.2:g.61392311G>T GRCh38
NC_000011.9:g.61159783G>T , CM000673.1:g.61159783G>T GRCh37
NC_000011.8:g.60916359G>T NCBI36
NG_032976.1:g.4952G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-321G>T ENSP00000440638.1:n.-321G>T
XM_005274039.3:c.-652G>T XP_005274096.1:n.-652G>T
XM_005274039.4:c.-652G>T XP_005274096.1:n.-652G>T
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