Canonical Allele Identifier: CA260917436
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs1009742775
gnomAD v2: 14-52788990-T-G
gnomAD v3: 14-52322272-T-G
gnomAD v4: 14-52322272-T-G
MyVariant Identifiers: chr14:g.52788990T>G (hg19) chr14:g.52322272T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322272T>G , CM000676.2:g.52322272T>G GRCh38
NC_000014.8:g.52788990T>G , CM000676.1:g.52788990T>G GRCh37
NC_000014.7:g.51858740T>G NCBI36
NG_013082.1:g.12975T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4949T>G MANE Select ENSP00000245457.5:n.844-4949T>G
ENST00000245457.5:c.844-4949T>G ENSP00000245457.5:n.844-4949T>G
ENST00000557436.1:c.79-4949T>G ENSP00000450933.1:n.79-4949T>G
NM_000956.3:c.844-4949T>G NP_000947.2:n.844-4949T>G
NM_000956.4:c.844-4949T>G MANE Select NP_000947.2:n.844-4949T>G
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