Canonical Allele Identifier: CA613904704

Gene: PTGER2

Linked Data

• dbSNP Id: rs940091249
• gnomAD v2: 14-52788889-G-C
• gnomAD v3: 14-52322171-G-C
• gnomAD v4: 14-52322171-G-C
• MyVariant Identifiers: chr14:g.52788889G>C (hg19) ; chr14:g.52322171G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52322171G>C , CM000676.2:g.52322171G>C	GRCh38
NC_000014.8:g.52788889G>C , CM000676.1:g.52788889G>C	GRCh37
NC_000014.7:g.51858639G>C	NCBI36
NG_013082.1:g.12874G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245457.6:c.844-5050G>C MANE Select	ENSP00000245457.5:n.844-5050G>C
ENST00000245457.5:c.844-5050G>C	ENSP00000245457.5:n.844-5050G>C
ENST00000557436.1:c.79-5050G>C	ENSP00000450933.1:n.79-5050G>C
NM_000956.3:c.844-5050G>C	NP_000947.2:n.844-5050G>C
NM_000956.4:c.844-5050G>C MANE Select	NP_000947.2:n.844-5050G>C