Canonical Allele Identifier: CA367788074
Gene: BAZ1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.72857056T>A (hg19) chr7:g.73442726T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73442726T>A , CM000669.2:g.73442726T>A GRCh38
NC_000007.13:g.72857056T>A , CM000669.1:g.72857056T>A GRCh37
NC_000007.12:g.72494992T>A NCBI36
NG_027679.1:g.84560A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000339594.9:c.4093A>T MANE Select ENSP00000342434.4:p.Arg1365Trp
ENST00000339594.8:c.4093A>T ENSP00000342434.4:p.Arg1365Trp
ENST00000404251.1:c.4093A>T ENSP00000385442.1:p.Arg1365Trp
NM_032408.3:c.4093A>T NP_115784.1:p.Arg1365Trp
XM_017012773.2:c.4093A>T XP_016868262.1:p.Arg1365Trp
NM_032408.4:c.4093A>T MANE Select NP_115784.1:p.Arg1365Trp
NM_001370402.1:c.4093A>T NP_001357331.1:p.Arg1365Trp
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