Canonical Allele Identifier: CA346475857
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29071189-C-T
MyVariant Identifiers: chr2:g.29294055C>T (hg19) chr2:g.29071189C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071189C>T , CM000664.2:g.29071189C>T GRCh38
NC_000002.11:g.29294055C>T , CM000664.1:g.29294055C>T GRCh37
NC_000002.10:g.29147559C>T NCBI36
NG_021427.1:g.8073G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3073G>A MANE Select ENSP00000332809.4:p.Ala1025Thr
ENST00000331664.5:c.3073G>A ENSP00000332809.4:p.Ala1025Thr
NM_001029883.2:c.3073G>A NP_001025054.1:p.Ala1025Thr
XM_011532826.1:c.3073G>A XP_011531128.1:p.Ala1025Thr
XR_939901.1:n.185+2022C>T
XR_939902.1:n.173+2034C>T
NM_001029883.3:c.3073G>A MANE Select NP_001025054.1:p.Ala1025Thr
Search 100 bp 5'
Search 100 bp 3'