Canonical Allele Identifier: CA497668127
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1435455130
gnomAD v2: 17-4535250-G-C
gnomAD v3: 17-4631955-G-C
gnomAD v4: 17-4631955-G-C
MyVariant Identifiers: chr17:g.4535250G>C (hg19) chr17:g.4631955G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631955G>C , CM000679.2:g.4631955G>C GRCh38
NC_000017.10:g.4535250G>C , CM000679.1:g.4535250G>C GRCh37
NC_000017.9:g.4481999G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1743C>G MANE Select ENSP00000293761.3:p.Pro581=
ENST00000570836.6:c.1743C>G ENSP00000458832.1:p.Pro581=
ENST00000293761.7:c.1743C>G ENSP00000293761.3:p.Pro581=
ENST00000570836.5:c.1743C>G ENSP00000458832.1:p.Pro581=
ENST00000574640.1:c.1626C>G ENSP00000460483.1:p.Pro542=
NM_001140.3:c.1743C>G NP_001131.3:p.Pro581=
NM_001140.4:c.1743C>G NP_001131.3:p.Pro581=
NM_001140.5:c.1743C>G MANE Select NP_001131.3:p.Pro581=
Search 100 bp 5'
Search 100 bp 3'