Canonical Allele Identifier: CA1937420419
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1565101141
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570912G>T , CM000672.2:g.113570912G>T GRCh38
NC_000010.10:g.115330671G>T , CM000672.1:g.115330671G>T GRCh37
NC_000010.9:g.115320661G>T NCBI36
NG_008956.1:g.22894G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.107-3377G>T MANE Select ENSP00000277903.4:n.107-3377G>T
ENST00000351270.3:c.107-3377G>T ENSP00000277903.4:n.107-3377G>T
ENST00000542051.5:c.29-3377G>T ENSP00000443283.1:n.29-3377G>T
NM_001177660.1:c.29-3377G>T NP_001171131.1:n.29-3377G>T
NM_004132.3:c.107-3377G>T NP_004123.1:n.107-3377G>T
NM_001177660.2:c.29-3377G>T NP_001171131.1:n.29-3377G>T
NM_004132.4:c.107-3377G>T NP_004123.1:n.107-3377G>T
NM_004132.5:c.107-3377G>T MANE Select NP_004123.1:n.107-3377G>T
NM_001177660.3:c.29-3377G>T NP_001171131.1:n.29-3377G>T
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