Canonical Allele Identifier: CA1591241151
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs1014713042
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101097A>T , CM000667.2:g.151101097A>T GRCh38
NC_000005.9:g.150480658A>T , CM000667.1:g.150480658A>T GRCh37
NC_000005.8:g.150460851A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*351T>A MANE Select ENSP00000346550.5:n.*351T>A
ENST00000522664.5:c.201-135T>A
NM_001155.4:c.*351T>A NP_001146.2:n.*351T>A
NM_001193544.1:c.*351T>A NP_001180473.1:n.*351T>A
NM_001363114.1:c.*351T>A NP_001350043.1:n.*351T>A
NM_001155.5:c.*351T>A MANE Select NP_001146.2:n.*351T>A
NM_001193544.2:c.*351T>A NP_001180473.1:n.*351T>A
NM_001363114.2:c.*351T>A NP_001350043.1:n.*351T>A
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