Canonical Allele Identifier: CA44639228
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs375826049
gnomAD v2: 2-29293598-C-A
gnomAD v3: 2-29070732-C-A
gnomAD v4: 2-29070732-C-A
MyVariant Identifiers: chr2:g.29293598C>A (hg19) chr2:g.29070732C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070732C>A , CM000664.2:g.29070732C>A GRCh38
NC_000002.11:g.29293598C>A , CM000664.1:g.29293598C>A GRCh37
NC_000002.10:g.29147102C>A NCBI36
NG_021427.1:g.8530G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3530G>T MANE Select ENSP00000332809.4:p.Arg1177Leu
ENST00000331664.5:c.3530G>T ENSP00000332809.4:p.Arg1177Leu
NM_001029883.2:c.3530G>T NP_001025054.1:p.Arg1177Leu
XM_011532826.1:c.3530G>T XP_011531128.1:p.Arg1177Leu
XR_939901.1:n.185+1565C>A
XR_939902.1:n.173+1577C>A
NM_001029883.3:c.3530G>T MANE Select NP_001025054.1:p.Arg1177Leu
Search 100 bp 5'
Search 100 bp 3'