Canonical Allele Identifier: CA346472943
Gene: PCARE HGNC NCBI

Linked Data

dbSNP Id: rs370727666
MyVariant Identifiers: chr2:g.29293587G>T (hg19) chr2:g.29070721G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070721G>T , CM000664.2:g.29070721G>T GRCh38
NC_000002.11:g.29293587G>T , CM000664.1:g.29293587G>T GRCh37
NC_000002.10:g.29147091G>T NCBI36
NG_021427.1:g.8541C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3541C>A MANE Select ENSP00000332809.4:p.Leu1181Met
ENST00000331664.5:c.3541C>A ENSP00000332809.4:p.Leu1181Met
NM_001029883.2:c.3541C>A NP_001025054.1:p.Leu1181Met
XM_011532826.1:c.3541C>A XP_011531128.1:p.Leu1181Met
XR_939901.1:n.185+1554G>T
XR_939902.1:n.173+1566G>T
NM_001029883.3:c.3541C>A MANE Select NP_001025054.1:p.Leu1181Met
Search 100 bp 5'
Search 100 bp 3'