Canonical Allele Identifier: CA163066099
Gene: BAIAP2L1 HGNC NCBI

Linked Data

dbSNP Id: rs979683885
MyVariant Identifiers: chr7:g.98021162C>T (hg19) chr7:g.98391850C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98391850C>T , CM000669.2:g.98391850C>T GRCh38
NC_000007.13:g.98021162C>T , CM000669.1:g.98021162C>T GRCh37
NC_000007.12:g.97859098C>T NCBI36
NG_013090.1:g.14266G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000005260.9:c.51+8952G>A MANE Select ENSP00000005260.8:n.51+8952G>A
ENST00000005260.8:c.51+8952G>A ENSP00000005260.8:n.51+8952G>A
ENST00000462558.5:n.267+8952G>A
ENST00000479789.1:n.357+8131G>A
NM_018842.4:c.51+8952G>A NP_061330.2:n.51+8952G>A
NM_018842.5:c.51+8952G>A MANE Select NP_061330.2:n.51+8952G>A
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