Canonical Allele Identifier: CA379724669

Gene: PTH

Linked Data

• MyVariant Identifiers: chr11:g.13514120C>A (hg19) ; chr11:g.13492573C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13492573C>A , CM000673.2:g.13492573C>A	GRCh38
NC_000011.9:g.13514120C>A , CM000673.1:g.13514120C>A	GRCh37
NC_000011.8:g.13470696C>A	NCBI36
NG_008962.1:g.8448G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282091.6:c.180G>T MANE Select	ENSP00000282091.1:p.Gln60His
ENST00000282091.5:c.180G>T	ENSP00000282091.1:p.Gln60His
ENST00000529816.1:c.180G>T	ENSP00000433208.1:p.Gln60His
NM_000315.2:c.180G>T	NP_000306.1:p.Gln60His
NM_000315.3:c.180G>T	NP_000306.1:p.Gln60His
NM_001316352.1:c.276G>T	NP_001303281.1:p.Gln92His
NM_000315.4:c.180G>T MANE Select	NP_000306.1:p.Gln60His
NM_001316352.2:c.276G>T	NP_001303281.1:p.Gln92His