Canonical Allele Identifier: CA2625129197
Gene: SIX1 HGNC NCBI

Linked Data

gnomAD v4: 14-60649479-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649479G>A , CM000676.2:g.60649479G>A GRCh38
NC_000014.8:g.61116197G>A , CM000676.1:g.61116197G>A GRCh37
NC_000014.7:g.60185950G>A NCBI36
NG_008231.1:g.4959C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2456C>T
ENST00000554986.2:c.42-2902C>T ENSP00000452700.2:n.42-2902C>T
ENST00000555955.3:n.1197+2456C>T
XM_017021602.2:c.-290C>T XP_016877091.1:n.-290C>T
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