Canonical Allele Identifier: CA346472818
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29070657-C-A
MyVariant Identifiers: chr2:g.29293523C>A (hg19) chr2:g.29070657C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070657C>A , CM000664.2:g.29070657C>A GRCh38
NC_000002.11:g.29293523C>A , CM000664.1:g.29293523C>A GRCh37
NC_000002.10:g.29147027C>A NCBI36
NG_021427.1:g.8605G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3605G>T MANE Select ENSP00000332809.4:p.Arg1202Leu
ENST00000331664.5:c.3605G>T ENSP00000332809.4:p.Arg1202Leu
NM_001029883.2:c.3605G>T NP_001025054.1:p.Arg1202Leu
XM_011532826.1:c.3605G>T XP_011531128.1:p.Arg1202Leu
XR_939901.1:n.185+1490C>A
XR_939902.1:n.173+1502C>A
NM_001029883.3:c.3605G>T MANE Select NP_001025054.1:p.Arg1202Leu
Search 100 bp 5'
Search 100 bp 3'