Canonical Allele Identifier: CA2734001902
Gene: SOX9 HGNC NCBI

Linked Data

dbSNP Id: rs2143249501
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72123470G>T , CM000679.2:g.72123470G>T GRCh38
NC_000017.10:g.70119611G>T , CM000679.1:g.70119611G>T GRCh37
NC_000017.9:g.67631206G>T NCBI36
NG_012490.1:g.7451G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000245479.3:c.686-73G>T MANE Select ENSP00000245479.2:n.686-73G>T
ENST00000245479.2:c.686-73G>T ENSP00000245479.2:n.686-73G>T
NM_000346.3:c.686-73G>T NP_000337.1:n.686-73G>T
NM_000346.4:c.686-73G>T MANE Select NP_000337.1:n.686-73G>T
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Search 100 bp 3'