Canonical Allele Identifier: CA2662659620
Gene: TMEM237 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201621152C>A , CM000664.2:g.201621152C>A GRCh38
NC_000002.11:g.202485875C>A , CM000664.1:g.202485875C>A GRCh37
NC_000002.10:g.202194120C>A NCBI36
NG_032049.1:g.27378G>T
NG_051007.1:g.3031G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000621467.5:c.*3103G>T ENSP00000480508.2:n.*3103G>T
ENST00000686475.1:n.4270G>T
ENST00000409883.7:c.*3103G>T MANE Select ENSP00000386264.2:n.*3103G>T
ENST00000409444.6:c.*3103G>T ENSP00000387203.2:n.*3103G>T
ENST00000409883.6:c.*3103G>T ENSP00000386264.2:n.*3103G>T
ENST00000495329.1:n.3469G>T
NM_001044385.2:c.*3103G>T NP_001037850.1:n.*3103G>T
NM_152388.3:c.*3103G>T NP_689601.2:n.*3103G>T
NM_001044385.3:c.*3103G>T MANE Select NP_001037850.1:n.*3103G>T
NM_152388.4:c.*3103G>T NP_689601.2:n.*3103G>T