Canonical Allele Identifier: CA425616594
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29071016-G-T
MyVariant Identifiers: chr2:g.29293882G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071016G>T , CM000664.2:g.29071016G>T GRCh38
NC_000002.11:g.29293882G>T , CM000664.1:g.29293882G>T GRCh37
NC_000002.10:g.29147386G>T NCBI36
NG_021427.1:g.8246C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3246C>A MANE Select ENSP00000332809.4:p.Pro1082=
ENST00000331664.5:c.3246C>A ENSP00000332809.4:p.Pro1082=
NM_001029883.2:c.3246C>A NP_001025054.1:p.Pro1082=
XM_011532826.1:c.3246C>A XP_011531128.1:p.Pro1082=
XR_939901.1:n.185+1849G>T
XR_939902.1:n.173+1861G>T
NM_001029883.3:c.3246C>A MANE Select NP_001025054.1:p.Pro1082=
Search 100 bp 5'
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