Canonical Allele Identifier: CA181484922
Gene: GDF6 HGNC NCBI

Linked Data

dbSNP Id: rs1042799995
gnomAD v3: 8-96143890-T-C
gnomAD v4: 8-96143890-T-C
MyVariant Identifiers: chr8:g.97156118T>C (hg19) chr8:g.96143890T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96143890T>C , CM000670.2:g.96143890T>C GRCh38
NC_000008.10:g.97156118T>C , CM000670.1:g.97156118T>C GRCh37
NC_000008.9:g.97225294T>C NCBI36
NG_008981.1:g.21903A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.*673A>G MANE Select ENSP00000287020.4:n.*673A>G
ENST00000287020.6:c.*673A>G ENSP00000287020.4:n.*673A>G
NM_001001557.2:c.*673A>G NP_001001557.1:n.*673A>G
XM_011517030.1:c.*673A>G XP_011515332.1:n.*673A>G
NM_001001557.3:c.*673A>G NP_001001557.1:n.*673A>G
NM_001001557.4:c.*673A>G MANE Select NP_001001557.1:n.*673A>G
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