Canonical Allele Identifier: CA685786554
Gene: C12orf60 HGNC NCBI

Linked Data

dbSNP Id: rs1800799
gnomAD v3: 12-14886361-G-T
gnomAD v4: 12-14886361-G-T
MyVariant Identifiers: chr12:g.15039295G>T (hg19) chr12:g.14886361G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14886361G>T , CM000674.2:g.14886361G>T GRCh38
NC_000012.11:g.15039295G>T , CM000674.1:g.15039295G>T GRCh37
NC_000012.10:g.14930562G>T NCBI36
NG_023331.1:g.4559C>A
NG_023331.2:g.4559C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648334.1:n.126-17646G>T
ENST00000527783.1:n.76-12808G>T
ENST00000533472.1:n.87-17646G>T
ENST00000543822.1:n.91+555G>T
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