Canonical Allele Identifier: CA14774061
Gene: SRC HGNC NCBI

Linked Data

dbSNP Id: rs6017996
gnomAD v2: 20-35986653-G-A
gnomAD v3: 20-37358250-G-A
gnomAD v4: 20-37358250-G-A
MyVariant Identifiers: chr20:g.35986653G>A (hg19) chr20:g.37358250G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.37358250G>A , CM000682.2:g.37358250G>A GRCh38
NC_000020.10:g.35986653G>A , CM000682.1:g.35986653G>A GRCh37
NC_000020.9:g.35420067G>A NCBI36
NG_023033.1:g.18566G>A , LRG_1018:g.18566G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000692112.1:c.-246-6954G>A ENSP00000508666.1:n.-246-6954G>A
ENST00000692423.1:c.-364-6954G>A ENSP00000509325.1:n.-364-6954G>A
ENST00000693012.1:c.-246-6954G>A ENSP00000510370.1:n.-246-6954G>A
ENST00000373578.7:c.-246-6954G>A MANE Select ENSP00000362680.2:n.-246-6954G>A
ENST00000373578.6:c.-246-6954G>A ENSP00000362680.2:n.-246-6954G>A
ENST00000497734.5:n.204-6954G>A
NM_005417.4:c.-246-6954G>A NP_005408.1:n.-246-6954G>A
NM_198291.2:c.-246-6954G>A , LRG_1018t1:c.-246-6954G>A NP_938033.1:n.-246-6954G>A
XM_011529013.1:c.-246-6954G>A XP_011527315.1:n.-246-6954G>A
XM_011529013.2:c.-246-6954G>A XP_011527315.1:n.-246-6954G>A
XM_017028024.1:c.-246-6954G>A XP_016883513.1:n.-246-6954G>A
XM_017028025.1:c.-246-6954G>A XP_016883514.1:n.-246-6954G>A
XM_017028026.1:c.-246-6954G>A XP_016883515.1:n.-246-6954G>A
NM_005417.5:c.-246-6954G>A NP_005408.1:n.-246-6954G>A
NM_198291.3:c.-246-6954G>A MANE Select NP_938033.1:n.-246-6954G>A
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