Canonical Allele Identifier: CA214431661
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs749241333
MyVariant Identifiers: chr10:g.115330675G>A (hg19) chr10:g.113570916G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570916G>A , CM000672.2:g.113570916G>A GRCh38
NC_000010.10:g.115330675G>A , CM000672.1:g.115330675G>A GRCh37
NC_000010.9:g.115320665G>A NCBI36
NG_008956.1:g.22898G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.107-3373G>A MANE Select ENSP00000277903.4:n.107-3373G>A
ENST00000351270.3:c.107-3373G>A ENSP00000277903.4:n.107-3373G>A
ENST00000542051.5:c.29-3373G>A ENSP00000443283.1:n.29-3373G>A
NM_001177660.1:c.29-3373G>A NP_001171131.1:n.29-3373G>A
NM_004132.3:c.107-3373G>A NP_004123.1:n.107-3373G>A
NM_001177660.2:c.29-3373G>A NP_001171131.1:n.29-3373G>A
NM_004132.4:c.107-3373G>A NP_004123.1:n.107-3373G>A
NM_004132.5:c.107-3373G>A MANE Select NP_004123.1:n.107-3373G>A
NM_001177660.3:c.29-3373G>A NP_001171131.1:n.29-3373G>A
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