Canonical Allele Identifier: CA12594303
Gene: TMEM225B HGNC NCBI

Linked Data

dbSNP Id: rs1581492
gnomAD v2: 7-99186826-G-A
gnomAD v3: 7-99589203-G-A
gnomAD v4: 7-99589203-G-A
MyVariant Identifiers: chr7:g.99186826G>A (hg19) chr7:g.99589203G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99589203G>A , CM000669.2:g.99589203G>A GRCh38
NC_000007.13:g.99186826G>A , CM000669.1:g.99186826G>A GRCh37
NC_000007.12:g.99024762G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455905.1:c.137-11005G>A ENSP00000401282.1:n.137-11005G>A
ENST00000486324.2:n.257-11005G>A
XM_017011629.2:c.-202-8733G>A XP_016867118.1:n.-202-8733G>A
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