Canonical Allele Identifier: CA45691549
Gene: TMEM178A HGNC NCBI

Linked Data

dbSNP Id: rs999642337
MyVariant Identifiers: chr2:g.39947659A>G (hg19) chr2:g.39720519A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39720519A>G , CM000664.2:g.39720519A>G GRCh38
NC_000002.11:g.39947659A>G , CM000664.1:g.39947659A>G GRCh37
NC_000002.10:g.39801163A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_024452702.1:c.401-14710A>G XP_024308470.1:n.401-14710A>G
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