Canonical Allele Identifier: CA1977295392
Gene: TMEM216 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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