Canonical Allele Identifier: CA346480677
Gene: PCARE HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29295922G>C (hg19) chr2:g.29073056G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29073056G>C , CM000664.2:g.29073056G>C GRCh38
NC_000002.11:g.29295922G>C , CM000664.1:g.29295922G>C GRCh37
NC_000002.10:g.29149426G>C NCBI36
NG_021427.1:g.6206C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.1206C>G MANE Select ENSP00000332809.4:p.Phe402Leu
ENST00000331664.5:c.1206C>G ENSP00000332809.4:p.Phe402Leu
NM_001029883.2:c.1206C>G NP_001025054.1:p.Phe402Leu
XM_011532826.1:c.1206C>G XP_011531128.1:p.Phe402Leu
XR_939901.1:n.185+3889G>C
XR_939902.1:n.173+3901G>C
NM_001029883.3:c.1206C>G MANE Select NP_001025054.1:p.Phe402Leu
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