Canonical Allele Identifier: CA367788152
Gene: BAZ1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.72857065A>C (hg19) chr7:g.73442735A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73442735A>C , CM000669.2:g.73442735A>C GRCh38
NC_000007.13:g.72857065A>C , CM000669.1:g.72857065A>C GRCh37
NC_000007.12:g.72495001A>C NCBI36
NG_027679.1:g.84551T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000339594.9:c.4084T>G MANE Select ENSP00000342434.4:p.Trp1362Gly
ENST00000339594.8:c.4084T>G ENSP00000342434.4:p.Trp1362Gly
ENST00000404251.1:c.4084T>G ENSP00000385442.1:p.Trp1362Gly
NM_032408.3:c.4084T>G NP_115784.1:p.Trp1362Gly
XM_017012773.2:c.4084T>G XP_016868262.1:p.Trp1362Gly
NM_032408.4:c.4084T>G MANE Select NP_115784.1:p.Trp1362Gly
NM_001370402.1:c.4084T>G NP_001357331.1:p.Trp1362Gly
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