Canonical Allele Identifier: CA13977496

Gene: PTGER2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52316377G>T , CM000676.2:g.52316377G>T	GRCh38
NC_000014.8:g.52783095G>T , CM000676.1:g.52783095G>T	GRCh37
NC_000014.7:g.51852845G>T	NCBI36
NG_013082.1:g.7080G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245457.6:c.843+986G>T MANE Select	ENSP00000245457.5:n.843+986G>T
ENST00000245457.5:c.843+986G>T	ENSP00000245457.5:n.843+986G>T
ENST00000557436.1:c.78+986G>T	ENSP00000450933.1:n.78+986G>T
NM_000956.3:c.843+986G>T	NP_000947.2:n.843+986G>T
NM_000956.4:c.843+986G>T MANE Select	NP_000947.2:n.843+986G>T