Canonical Allele Identifier: CA425616667
Gene: PCARE HGNC NCBI

Linked Data

gnomAD v4: 2-29071058-G-A
MyVariant Identifiers: chr2:g.29293924G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071058G>A , CM000664.2:g.29071058G>A GRCh38
NC_000002.11:g.29293924G>A , CM000664.1:g.29293924G>A GRCh37
NC_000002.10:g.29147428G>A NCBI36
NG_021427.1:g.8204C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3204C>T MANE Select ENSP00000332809.4:p.Cys1068=
ENST00000331664.5:c.3204C>T ENSP00000332809.4:p.Cys1068=
NM_001029883.2:c.3204C>T NP_001025054.1:p.Cys1068=
XM_011532826.1:c.3204C>T XP_011531128.1:p.Cys1068=
XR_939901.1:n.185+1891G>A
XR_939902.1:n.173+1903G>A
NM_001029883.3:c.3204C>T MANE Select NP_001025054.1:p.Cys1068=