Canonical Allele Identifier: CA706696288
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs1281556749
gnomAD v3: 14-52321823-A-G
gnomAD v4: 14-52321823-A-G
MyVariant Identifiers: chr14:g.52788541A>G (hg19) chr14:g.52321823A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52321823A>G , CM000676.2:g.52321823A>G GRCh38
NC_000014.8:g.52788541A>G , CM000676.1:g.52788541A>G GRCh37
NC_000014.7:g.51858291A>G NCBI36
NG_013082.1:g.12526A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-5398A>G MANE Select ENSP00000245457.5:n.844-5398A>G
ENST00000245457.5:c.844-5398A>G ENSP00000245457.5:n.844-5398A>G
ENST00000557436.1:c.79-5398A>G ENSP00000450933.1:n.79-5398A>G
NM_000956.3:c.844-5398A>G NP_000947.2:n.844-5398A>G
NM_000956.4:c.844-5398A>G MANE Select NP_000947.2:n.844-5398A>G
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