Canonical Allele Identifier: CA1977295408
Gene: TMEM216 HGNC NCBI

Linked Data

dbSNP Id: rs1590640785

Genomic Alleles

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

Transcript Alleles

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