Canonical Allele Identifier: CA163066137
Gene: BAIAP2L1 HGNC NCBI

Linked Data

dbSNP Id: rs181377431
gnomAD v2: 7-98021232-T-C
gnomAD v3: 7-98391920-T-C
gnomAD v4: 7-98391920-T-C
MyVariant Identifiers: chr7:g.98021232T>C (hg19) chr7:g.98391920T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98391920T>C , CM000669.2:g.98391920T>C GRCh38
NC_000007.13:g.98021232T>C , CM000669.1:g.98021232T>C GRCh37
NC_000007.12:g.97859168T>C NCBI36
NG_013090.1:g.14196A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000005260.9:c.51+8882A>G MANE Select ENSP00000005260.8:n.51+8882A>G
ENST00000005260.8:c.51+8882A>G ENSP00000005260.8:n.51+8882A>G
ENST00000462558.5:n.267+8882A>G
ENST00000479789.1:n.357+8061A>G
NM_018842.4:c.51+8882A>G NP_061330.2:n.51+8882A>G
NM_018842.5:c.51+8882A>G MANE Select NP_061330.2:n.51+8882A>G
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