Canonical Allele Identifier: CA378422191
Gene: HABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.115348046G>C (hg19) chr10:g.113588287G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588287G>C , CM000672.2:g.113588287G>C GRCh38
NC_000010.10:g.115348046G>C , CM000672.1:g.115348046G>C GRCh37
NC_000010.9:g.115338036G>C NCBI36
NG_008956.1:g.40269G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.1601G>C MANE Select ENSP00000277903.4:p.Gly534Ala
ENST00000351270.3:c.1601G>C ENSP00000277903.4:p.Gly534Ala
ENST00000542051.5:c.1523G>C ENSP00000443283.1:p.Gly508Ala
NM_001177660.1:c.1523G>C NP_001171131.1:p.Gly508Ala
NM_004132.3:c.1601G>C NP_004123.1:p.Gly534Ala
NM_001177660.2:c.1523G>C NP_001171131.1:p.Gly508Ala
NM_004132.4:c.1601G>C NP_004123.1:p.Gly534Ala
NM_004132.5:c.1601G>C MANE Select NP_004123.1:p.Gly534Ala
NM_001177660.3:c.1523G>C NP_001171131.1:p.Gly508Ala
Search 100 bp 5'
Search 100 bp 3'