Canonical Allele Identifier: CA103381331
Gene:

Linked Data

dbSNP Id: rs960799307
gnomAD v3: 4-105542920-T-C
gnomAD v4: 4-105542920-T-C
MyVariant Identifiers: chr4:g.106464077T>C (hg19) chr4:g.105542920T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542920T>C , CM000666.2:g.105542920T>C GRCh38
NC_000004.11:g.106464077T>C , CM000666.1:g.106464077T>C GRCh37
NC_000004.10:g.106683526T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.296-211A>G
XR_939039.1:n.456-211A>G
XR_939040.1:n.296-1444A>G
XR_001741410.1:n.311-211A>G
XR_001741411.1:n.787-211A>G
XR_001741412.1:n.311-211A>G
XR_001741413.1:n.311-211A>G
XR_001741414.1:n.311-211A>G
XR_939038.2:n.311-211A>G
XR_939040.2:n.311-1444A>G
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