Canonical Allele Identifier: CA1977295394
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1051402574
gnomAD v3: 11-61392335-C-A
gnomAD v4: 11-61392335-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392335C>A , CM000673.2:g.61392335C>A GRCh38
NC_000011.9:g.61159807C>A , CM000673.1:g.61159807C>A GRCh37
NC_000011.8:g.60916383C>A NCBI36
NG_032976.1:g.4976C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-297C>A ENSP00000440638.1:n.-297C>A
XM_005274039.3:c.-628C>A XP_005274096.1:n.-628C>A
XM_005274039.4:c.-628C>A XP_005274096.1:n.-628C>A
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