Canonical Allele Identifier: CA7212889
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs757701604
ExAC: 14:61115943 C / T
gnomAD v2: 14-61115943-C-T
gnomAD v4: 14-60649225-C-T
MyVariant Identifiers: chr14:g.61115943C>T (hg19) chr14:g.60649225C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649225C>T , CM000676.2:g.60649225C>T GRCh38
NC_000014.8:g.61115943C>T , CM000676.1:g.61115943C>T GRCh37
NC_000014.7:g.60185696C>T NCBI36
NG_008231.1:g.5213G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.-36G>A MANE Select ENSP00000494686.1:n.-36G>A
ENST00000247182.6:c.-36G>A ENSP00000247182.5:n.-36G>A
ENST00000553535.2:n.249-2648G>A
ENST00000554986.2:c.42-2648G>A ENSP00000452700.2:n.42-2648G>A
ENST00000555955.3:n.1198-2648G>A
NM_005982.3:c.-36G>A NP_005973.1:n.-36G>A
XM_017021602.2:c.-36G>A XP_016877091.1:n.-36G>A
NM_005982.4:c.-36G>A MANE Select NP_005973.1:n.-36G>A
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