Canonical Allele Identifier: CA379724511
Gene: PTH HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.13514043T>C (hg19) chr11:g.13492496T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13492496T>C , CM000673.2:g.13492496T>C GRCh38
NC_000011.9:g.13514043T>C , CM000673.1:g.13514043T>C GRCh37
NC_000011.8:g.13470619T>C NCBI36
NG_008962.1:g.8525A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282091.6:c.257A>G MANE Select ENSP00000282091.1:p.Glu86Gly
ENST00000282091.5:c.257A>G ENSP00000282091.1:p.Glu86Gly
ENST00000529816.1:c.257A>G ENSP00000433208.1:p.Glu86Gly
NM_000315.2:c.257A>G NP_000306.1:p.Glu86Gly
NM_000315.3:c.257A>G NP_000306.1:p.Glu86Gly
NM_001316352.1:c.353A>G NP_001303281.1:p.Glu118Gly
NM_000315.4:c.257A>G MANE Select NP_000306.1:p.Glu86Gly
NM_001316352.2:c.353A>G NP_001303281.1:p.Glu118Gly
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