Canonical Allele Identifier: CA367787661
Gene: BAZ1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.72856857T>C (hg19) chr7:g.73442527T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73442527T>C , CM000669.2:g.73442527T>C GRCh38
NC_000007.13:g.72856857T>C , CM000669.1:g.72856857T>C GRCh37
NC_000007.12:g.72494793T>C NCBI36
NG_027679.1:g.84759A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339594.9:c.4121A>G MANE Select ENSP00000342434.4:p.Glu1374Gly
ENST00000339594.8:c.4121A>G ENSP00000342434.4:p.Glu1374Gly
ENST00000404251.1:c.4121A>G ENSP00000385442.1:p.Glu1374Gly
NM_032408.3:c.4121A>G NP_115784.1:p.Glu1374Gly
XM_017012773.2:c.4121A>G XP_016868262.1:p.Glu1374Gly
NM_032408.4:c.4121A>G MANE Select NP_115784.1:p.Glu1374Gly
NM_001370402.1:c.4121A>G NP_001357331.1:p.Glu1374Gly
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Search 100 bp 3'