Canonical Allele Identifier: CA706696604
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs1201886076
gnomAD v3: 14-52322374-G-T
gnomAD v4: 14-52322374-G-T
MyVariant Identifiers: chr14:g.52789092G>T (hg19) chr14:g.52322374G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52322374G>T , CM000676.2:g.52322374G>T GRCh38
NC_000014.8:g.52789092G>T , CM000676.1:g.52789092G>T GRCh37
NC_000014.7:g.51858842G>T NCBI36
NG_013082.1:g.13077G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245457.6:c.844-4847G>T MANE Select ENSP00000245457.5:n.844-4847G>T
ENST00000245457.5:c.844-4847G>T ENSP00000245457.5:n.844-4847G>T
ENST00000557436.1:c.79-4847G>T ENSP00000450933.1:n.79-4847G>T
NM_000956.3:c.844-4847G>T NP_000947.2:n.844-4847G>T
NM_000956.4:c.844-4847G>T MANE Select NP_000947.2:n.844-4847G>T
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