Canonical Allele Identifier: CA346475842
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29294048T>A (hg19) chr2:g.29071182T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29071182T>A , CM000664.2:g.29071182T>A GRCh38
NC_000002.11:g.29294048T>A , CM000664.1:g.29294048T>A GRCh37
NC_000002.10:g.29147552T>A NCBI36
NG_021427.1:g.8080A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000331664.6:c.3080A>T MANE Select ENSP00000332809.4:p.Gln1027Leu
ENST00000331664.5:c.3080A>T ENSP00000332809.4:p.Gln1027Leu
NM_001029883.2:c.3080A>T NP_001025054.1:p.Gln1027Leu
XM_011532826.1:c.3080A>T XP_011531128.1:p.Gln1027Leu
XR_939901.1:n.185+2015T>A
XR_939902.1:n.173+2027T>A
NM_001029883.3:c.3080A>T MANE Select NP_001025054.1:p.Gln1027Leu
Search 100 bp 5'
Search 100 bp 3'