Canonical Allele Identifier: CA440675902
Gene:

Linked Data

gnomAD v4: 4-105542617-G-T
MyVariant Identifiers: chr4:g.106463774G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542617G>T , CM000666.2:g.105542617G>T GRCh38
NC_000004.11:g.106463774G>T , CM000666.1:g.106463774G>T GRCh37
NC_000004.10:g.106683223G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.388C>A
XR_939039.1:n.548C>A
XR_939040.1:n.296-1141C>A
XR_001741410.1:n.403C>A
XR_001741411.1:n.879C>A
XR_001741412.1:n.403C>A
XR_001741413.1:n.403C>A
XR_001741414.1:n.403C>A
XR_939038.2:n.403C>A
XR_939040.2:n.311-1141C>A
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