Canonical Allele Identifier: CA2605429552
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs2113883892
gnomAD v3: 5-151100722-T-C
gnomAD v4: 5-151100722-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100722T>C , CM000667.2:g.151100722T>C GRCh38
NC_000005.9:g.150480283T>C , CM000667.1:g.150480283T>C GRCh37
NC_000005.8:g.150460476T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*726A>G MANE Select ENSP00000346550.5:n.*726A>G
ENST00000522664.5:c.441A>G
NM_001155.4:c.*726A>G NP_001146.2:n.*726A>G
NM_001193544.1:c.*726A>G NP_001180473.1:n.*726A>G
NM_001363114.1:c.*726A>G NP_001350043.1:n.*726A>G
NM_001155.5:c.*726A>G MANE Select NP_001146.2:n.*726A>G
NM_001193544.2:c.*726A>G NP_001180473.1:n.*726A>G
NM_001363114.2:c.*726A>G NP_001350043.1:n.*726A>G
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