Canonical Allele Identifier: CA1977295409
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1590640785

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392344A>G , CM000673.2:g.61392344A>G GRCh38
NC_000011.9:g.61159816A>G , CM000673.1:g.61159816A>G GRCh37
NC_000011.8:g.60916392A>G NCBI36
NG_032976.1:g.4985A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-288A>G ENSP00000440638.1:n.-288A>G
XM_005274039.3:c.-619A>G XP_005274096.1:n.-619A>G
XM_005274039.4:c.-619A>G XP_005274096.1:n.-619A>G