Canonical Allele Identifier: CA13977496
Gene: PTGER2 HGNC NCBI

Linked Data

dbSNP Id: rs45525634
gnomAD v2: 14-52783095-G-T
gnomAD v3: 14-52316377-G-T
gnomAD v4: 14-52316377-G-T
MyVariant Identifiers: chr14:g.52783095G>T (hg19) chr14:g.52783095_52783096delinsTT (hg19) chr14:g.52316377G>T (hg38) chr14:g.52316377_52316378delinsTT (hg38)
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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
Search 100 bp 5'
Search 100 bp 3'