Canonical Allele Identifier: CA260917500
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs773446279
gnomAD v2: 14-52789098-A-T
gnomAD v3: 14-52322380-A-T
gnomAD v4: 14-52322380-A-T
MyVariant Identifiers: chr14:g.52789098A>T (hg19) chr14:g.52322380A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322380A>T , CM000676.2:g.52322380A>T GRCh38
NC_000014.8:g.52789098A>T , CM000676.1:g.52789098A>T GRCh37
NC_000014.7:g.51858848A>T NCBI36
NG_013082.1:g.13083A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4841A>T MANE Select ENSP00000245457.5:n.844-4841A>T
ENST00000245457.5:c.844-4841A>T ENSP00000245457.5:n.844-4841A>T
ENST00000557436.1:c.79-4841A>T ENSP00000450933.1:n.79-4841A>T
NM_000956.3:c.844-4841A>T NP_000947.2:n.844-4841A>T
NM_000956.4:c.844-4841A>T MANE Select NP_000947.2:n.844-4841A>T
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