Canonical Allele Identifier: CA214431734
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs997002890

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113571081A>G , CM000672.2:g.113571081A>G GRCh38
NC_000010.10:g.115330840A>G , CM000672.1:g.115330840A>G GRCh37
NC_000010.9:g.115320830A>G NCBI36
NG_008956.1:g.23063A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.107-3208A>G MANE Select ENSP00000277903.4:n.107-3208A>G
ENST00000351270.3:c.107-3208A>G ENSP00000277903.4:n.107-3208A>G
ENST00000542051.5:c.29-3208A>G ENSP00000443283.1:n.29-3208A>G
NM_001177660.1:c.29-3208A>G NP_001171131.1:n.29-3208A>G
NM_004132.3:c.107-3208A>G NP_004123.1:n.107-3208A>G
NM_001177660.2:c.29-3208A>G NP_001171131.1:n.29-3208A>G
NM_004132.4:c.107-3208A>G NP_004123.1:n.107-3208A>G
NM_004132.5:c.107-3208A>G MANE Select NP_004123.1:n.107-3208A>G
NM_001177660.3:c.29-3208A>G NP_001171131.1:n.29-3208A>G