Canonical Allele Identifier: CA15678884
Gene: CORO1B HGNC NCBI
PTPRCAP HGNC NCBI

Linked Data

dbSNP Id: rs869736
gnomAD v2: 11-67205462-C-A
gnomAD v3: 11-67437991-C-A
gnomAD v4: 11-67437991-C-A
MyVariant Identifiers: chr11:g.67205462C>A (hg19) chr11:g.67437991C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67437991C>A , CM000673.2:g.67437991C>A GRCh38
NC_000011.9:g.67205462C>A , CM000673.1:g.67205462C>A GRCh37
NC_000011.8:g.66962038C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000341356.10:c.*385G>T (CORO1B) MANE Select ENSP00000340211.5:n.*385G>T
ENST00000326294.3:c.-372G>T (PTPRCAP) ENSP00000325589.3:n.-372G>T
ENST00000616321.4:c.*1117G>T (CORO1B) ENSP00000479949.1:n.*1117G>T
XR_950232.1:n.1120C>A
NM_020441.3:c.*385G>T (CORO1B) MANE Select NP_065174.1:n.*385G>T
NM_001018070.3:c.*385G>T (CORO1B) NP_001018080.1:n.*385G>T
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