Canonical Allele Identifier: CA245297469
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs988732152
MyVariant Identifiers: chr12:g.128702051C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128702051C>A , CM000674.2:g.128702051C>A GRCh38
NC_000012.11:g.129186596C>A , CM000674.1:g.129186596C>A GRCh37
NC_000012.10:g.127752549C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.2122-3039C>A MANE Select ENSP00000410852.2:n.2122-3039C>A
ENST00000435159.2:c.2122-3039C>A ENSP00000410852.2:n.2122-3039C>A
NM_001136103.2:c.2122-3039C>A NP_001129575.2:n.2122-3039C>A
XM_011538998.1:c.2062-3039C>A XP_011537300.1:n.2062-3039C>A
XM_011538998.2:c.2062-3039C>A XP_011537300.1:n.2062-3039C>A
XR_001748922.1:n.2355-2601C>A
NM_001136103.3:c.2122-3039C>A MANE Select NP_001129575.2:n.2122-3039C>A
NM_001387058.1:c.2062-3039C>A NP_001373987.1:n.2062-3039C>A
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