Canonical Allele Identifier: CA377145180
Gene: CHST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73767397T>C (hg19) chr10:g.72007639T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007639T>C , CM000672.2:g.72007639T>C GRCh38
NC_000010.10:g.73767397T>C , CM000672.1:g.73767397T>C GRCh37
NC_000010.9:g.73437403T>C NCBI36
NG_012635.1:g.48278T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.608T>C MANE Select ENSP00000362207.4:p.Leu203Pro
ENST00000373115.4:c.608T>C ENSP00000362207.4:p.Leu203Pro
NM_004273.4:c.608T>C NP_004264.2:p.Leu203Pro
XM_006718075.2:c.608T>C XP_006718138.1:p.Leu203Pro
XM_011540369.1:c.608T>C XP_011538671.1:p.Leu203Pro
XM_006718075.4:c.608T>C XP_006718138.1:p.Leu203Pro
XM_011540369.2:c.608T>C XP_011538671.1:p.Leu203Pro
NM_004273.5:c.608T>C MANE Select NP_004264.2:p.Leu203Pro
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