Canonical Allele Identifier: CA462454996
Gene: GDF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.97157517G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96145289G>C , CM000670.2:g.96145289G>C GRCh38
NC_000008.10:g.97157517G>C , CM000670.1:g.97157517G>C GRCh37
NC_000008.9:g.97226693G>C NCBI36
NG_008981.1:g.20504C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000287020.7:c.642C>G MANE Select ENSP00000287020.4:p.Val214=
ENST00000287020.6:c.642C>G ENSP00000287020.4:p.Val214=
ENST00000620978.1:c.642C>G ENSP00000480170.1:p.Val214=
ENST00000621429.1:c.642C>G ENSP00000483711.1:p.Val214=
NM_001001557.2:c.642C>G NP_001001557.1:p.Val214=
XM_011517030.1:c.243C>G XP_011515332.1:p.Val81=
NM_001001557.3:c.642C>G NP_001001557.1:p.Val214=
NM_001001557.4:c.642C>G MANE Select NP_001001557.1:p.Val214=