Canonical Allele Identifier: CA2676049729
Gene: ANXA6 HGNC NCBI

Linked Data

gnomAD v4: 5-151100961-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100961G>T , CM000667.2:g.151100961G>T GRCh38
NC_000005.9:g.150480522G>T , CM000667.1:g.150480522G>T GRCh37
NC_000005.8:g.150460715G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000354546.10:c.*487C>A MANE Select ENSP00000346550.5:n.*487C>A
ENST00000522664.5:c.202C>A
NM_001155.4:c.*487C>A NP_001146.2:n.*487C>A
NM_001193544.1:c.*487C>A NP_001180473.1:n.*487C>A
NM_001363114.1:c.*487C>A NP_001350043.1:n.*487C>A
NM_001155.5:c.*487C>A MANE Select NP_001146.2:n.*487C>A
NM_001193544.2:c.*487C>A NP_001180473.1:n.*487C>A
NM_001363114.2:c.*487C>A NP_001350043.1:n.*487C>A
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