Canonical Allele Identifier: CA163072689
Gene: BAIAP2L1 HGNC NCBI

Linked Data

dbSNP Id: rs531242568
gnomAD v3: 7-98363961-G-A
gnomAD v4: 7-98363961-G-A
MyVariant Identifiers: chr7:g.97993273G>A (hg19) chr7:g.98363961G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98363961G>A , CM000669.2:g.98363961G>A GRCh38
NC_000007.13:g.97993273G>A , CM000669.1:g.97993273G>A GRCh37
NC_000007.12:g.97831209G>A NCBI36
NG_013090.1:g.42155C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000005260.9:c.52-1529C>T MANE Select ENSP00000005260.8:n.52-1529C>T
ENST00000005260.8:c.52-1529C>T ENSP00000005260.8:n.52-1529C>T
ENST00000462558.5:n.268-1529C>T
ENST00000479789.1:n.358-1529C>T
NM_018842.4:c.52-1529C>T NP_061330.2:n.52-1529C>T
NM_018842.5:c.52-1529C>T MANE Select NP_061330.2:n.52-1529C>T
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