Canonical Allele Identifier: CA425617669
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29295973T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073107T>C , CM000664.2:g.29073107T>C GRCh38
NC_000002.11:g.29295973T>C , CM000664.1:g.29295973T>C GRCh37
NC_000002.10:g.29149477T>C NCBI36
NG_021427.1:g.6155A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1155A>G MANE Select ENSP00000332809.4:p.Ser385=
ENST00000331664.5:c.1155A>G ENSP00000332809.4:p.Ser385=
NM_001029883.2:c.1155A>G NP_001025054.1:p.Ser385=
XM_011532826.1:c.1155A>G XP_011531128.1:p.Ser385=
XR_939901.1:n.185+3940T>C
XR_939902.1:n.173+3952T>C
NM_001029883.3:c.1155A>G MANE Select NP_001025054.1:p.Ser385=
Search 100 bp 5'
Search 100 bp 3'