Canonical Allele Identifier: CA214431807
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs959931637
MyVariant Identifiers: chr10:g.115330991T>C (hg19) chr10:g.113571232T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113571232T>C , CM000672.2:g.113571232T>C GRCh38
NC_000010.10:g.115330991T>C , CM000672.1:g.115330991T>C GRCh37
NC_000010.9:g.115320981T>C NCBI36
NG_008956.1:g.23214T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.107-3057T>C MANE Select ENSP00000277903.4:n.107-3057T>C
ENST00000351270.3:c.107-3057T>C ENSP00000277903.4:n.107-3057T>C
ENST00000542051.5:c.29-3057T>C ENSP00000443283.1:n.29-3057T>C
NM_001177660.1:c.29-3057T>C NP_001171131.1:n.29-3057T>C
NM_004132.3:c.107-3057T>C NP_004123.1:n.107-3057T>C
NM_001177660.2:c.29-3057T>C NP_001171131.1:n.29-3057T>C
NM_004132.4:c.107-3057T>C NP_004123.1:n.107-3057T>C
NM_004132.5:c.107-3057T>C MANE Select NP_004123.1:n.107-3057T>C
NM_001177660.3:c.29-3057T>C NP_001171131.1:n.29-3057T>C
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