Canonical Allele Identifier: CA1937419444
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1845254885
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113569096G>A , CM000672.2:g.113569096G>A GRCh38
NC_000010.10:g.115328855G>A , CM000672.1:g.115328855G>A GRCh37
NC_000010.9:g.115318845G>A NCBI36
NG_008956.1:g.21078G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.106+1571G>A MANE Select ENSP00000277903.4:n.106+1571G>A
ENST00000351270.3:c.106+1571G>A ENSP00000277903.4:n.106+1571G>A
ENST00000460714.1:n.43-548G>A
ENST00000542051.5:c.28+1571G>A ENSP00000443283.1:n.28+1571G>A
NM_001177660.1:c.28+1571G>A NP_001171131.1:n.28+1571G>A
NM_004132.3:c.106+1571G>A NP_004123.1:n.106+1571G>A
NM_001177660.2:c.28+1571G>A NP_001171131.1:n.28+1571G>A
NM_004132.4:c.106+1571G>A NP_004123.1:n.106+1571G>A
NM_004132.5:c.106+1571G>A MANE Select NP_004123.1:n.106+1571G>A
NM_001177660.3:c.28+1571G>A NP_001171131.1:n.28+1571G>A
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