Canonical Allele Identifier: CA889531508
Gene: GATAD2B HGNC NCBI

Linked Data

dbSNP Id: rs1348850076
MyVariant Identifiers: chr1:g.153769436G>C (hg19) chr1:g.153796960G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153796960G>C , CM000663.2:g.153796960G>C GRCh38
NC_000001.10:g.153769436G>C , CM000663.1:g.153769436G>C GRCh37
NC_000001.9:g.152036060G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637918.1:c.136-6884C>G
ENST00000427283.1:n.819+395G>C
XM_017003084.2:c.53+397G>C XP_016858573.1:n.53+397G>C
XM_017003085.2:c.53+397G>C XP_016858574.1:n.53+397G>C
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