Canonical Allele Identifier: CA842015608
Gene: BAZ1B HGNC NCBI

Linked Data

dbSNP Id: rs1254858605
gnomAD v3: 7-73441956-T-C
gnomAD v4: 7-73441956-T-C
MyVariant Identifiers: chr7:g.73441956T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73441956T>C , CM000669.2:g.73441956T>C GRCh38
NC_000007.13:g.72856286T>C , CM000669.1:g.72856286T>C GRCh37
NC_000007.12:g.72494222T>C NCBI36
NG_027679.1:g.85330A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000339594.9:c.*15+225A>G MANE Select ENSP00000342434.4:n.*15+225A>G
ENST00000339594.8:c.*15+225A>G ENSP00000342434.4:n.*15+225A>G
ENST00000404251.1:c.*240A>G ENSP00000385442.1:n.*240A>G
NM_032408.3:c.*15+225A>G NP_115784.1:n.*15+225A>G
XM_017012773.2:c.*240A>G XP_016868262.1:n.*240A>G
NM_032408.4:c.*15+225A>G MANE Select NP_115784.1:n.*15+225A>G
NM_001370402.1:c.*240A>G NP_001357331.1:n.*240A>G
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