Canonical Allele Identifier: CA440676019
Gene:

Linked Data

gnomAD v4: 4-105542659-C-A
MyVariant Identifiers: chr4:g.106463816C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542659C>A , CM000666.2:g.105542659C>A GRCh38
NC_000004.11:g.106463816C>A , CM000666.1:g.106463816C>A GRCh37
NC_000004.10:g.106683265C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.346G>T
XR_939039.1:n.506G>T
XR_939040.1:n.296-1183G>T
XR_001741410.1:n.361G>T
XR_001741411.1:n.837G>T
XR_001741412.1:n.361G>T
XR_001741413.1:n.361G>T
XR_001741414.1:n.361G>T
XR_939038.2:n.361G>T
XR_939040.2:n.311-1183G>T
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