Canonical Allele Identifier: CA660058738
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1196424573
MyVariant Identifiers: chr10:g.115328861C>A (hg19) chr10:g.113569102C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113569102C>A , CM000672.2:g.113569102C>A GRCh38
NC_000010.10:g.115328861C>A , CM000672.1:g.115328861C>A GRCh37
NC_000010.9:g.115318851C>A NCBI36
NG_008956.1:g.21084C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.106+1577C>A MANE Select ENSP00000277903.4:n.106+1577C>A
ENST00000351270.3:c.106+1577C>A ENSP00000277903.4:n.106+1577C>A
ENST00000460714.1:n.43-542C>A
ENST00000542051.5:c.28+1577C>A ENSP00000443283.1:n.28+1577C>A
NM_001177660.1:c.28+1577C>A NP_001171131.1:n.28+1577C>A
NM_004132.3:c.106+1577C>A NP_004123.1:n.106+1577C>A
NM_001177660.2:c.28+1577C>A NP_001171131.1:n.28+1577C>A
NM_004132.4:c.106+1577C>A NP_004123.1:n.106+1577C>A
NM_004132.5:c.106+1577C>A MANE Select NP_004123.1:n.106+1577C>A
NM_001177660.3:c.28+1577C>A NP_001171131.1:n.28+1577C>A
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