Canonical Allele Identifier: CA346475579
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29071047-C-G
MyVariant Identifiers: chr2:g.29293913C>G (hg19) chr2:g.29071047C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071047C>G , CM000664.2:g.29071047C>G GRCh38
NC_000002.11:g.29293913C>G , CM000664.1:g.29293913C>G GRCh37
NC_000002.10:g.29147417C>G NCBI36
NG_021427.1:g.8215G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3215G>C MANE Select ENSP00000332809.4:p.Ser1072Thr
ENST00000331664.5:c.3215G>C ENSP00000332809.4:p.Ser1072Thr
NM_001029883.2:c.3215G>C NP_001025054.1:p.Ser1072Thr
XM_011532826.1:c.3215G>C XP_011531128.1:p.Ser1072Thr
XR_939901.1:n.185+1880C>G
XR_939902.1:n.173+1892C>G
NM_001029883.3:c.3215G>C MANE Select NP_001025054.1:p.Ser1072Thr
Search 100 bp 5'
Search 100 bp 3'