Canonical Allele Identifier: CA1937420608
Gene: HABP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113571282T= , CM000672.2:g.113571282T= GRCh38
NC_000010.10:g.115331041T= , CM000672.1:g.115331041T= GRCh37
NC_000010.9:g.115321031T= NCBI36
NG_008956.1:g.23264T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.107-3007T= MANE Select ENSP00000277903.4:n.107-3007T=
ENST00000351270.3:c.107-3007T= ENSP00000277903.4:n.107-3007T=
ENST00000542051.5:c.29-3007T= ENSP00000443283.1:n.29-3007T=
NM_001177660.1:c.29-3007T= NP_001171131.1:n.29-3007T=
NM_004132.3:c.107-3007T= NP_004123.1:n.107-3007T=
NM_001177660.2:c.29-3007T= NP_001171131.1:n.29-3007T=
NM_004132.4:c.107-3007T= NP_004123.1:n.107-3007T=
NM_004132.5:c.107-3007T= MANE Select NP_004123.1:n.107-3007T=
NM_001177660.3:c.29-3007T= NP_001171131.1:n.29-3007T=
Search 100 bp 5'
Search 100 bp 3'