Canonical Allele Identifier: CA440675805
Gene:

Linked Data

dbSNP Id: rs1724781095
MyVariant Identifiers: chr4:g.106463741A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542584A>T , CM000666.2:g.105542584A>T GRCh38
NC_000004.11:g.106463741A>T , CM000666.1:g.106463741A>T GRCh37
NC_000004.10:g.106683190A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.421T>A
XR_939039.1:n.581T>A
XR_939040.1:n.296-1108T>A
XR_001741410.1:n.436T>A
XR_001741411.1:n.912T>A
XR_001741412.1:n.436T>A
XR_001741413.1:n.436T>A
XR_001741414.1:n.436T>A
XR_939038.2:n.436T>A
XR_939040.2:n.311-1108T>A
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