Canonical Allele Identifier: CA2184234552
Gene: SMAD6 HGNC NCBI

Linked Data

dbSNP Id: rs1595804482

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66780895A>C , CM000677.2:g.66780895A>C GRCh38
NC_000015.9:g.67073233A>C , CM000677.1:g.67073233A>C GRCh37
NC_000015.8:g.64860287A>C NCBI36
NG_012244.1:g.83560A>C
NG_012244.2:g.83560A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000288840.10:c.953-102A>C MANE Select ENSP00000288840.5:n.953-102A>C
ENST00000288840.9:c.953-102A>C ENSP00000288840.5:n.953-102A>C
ENST00000557916.5:c.1085-102A>C ENSP00000452955.1:n.1085-102A>C
ENST00000559931.5:c.257-102A>C ENSP00000453446.1:n.257-102A>C
NM_005585.4:c.953-102A>C NP_005576.3:n.953-102A>C
NR_027654.1:n.2008-102A>C
XM_011521561.1:c.170-102A>C XP_011519863.1:n.170-102A>C
XR_931825.1:n.2352-102A>C
XM_011521561.2:c.170-102A>C XP_011519863.1:n.170-102A>C
NM_005585.5:c.953-102A>C MANE Select NP_005576.3:n.953-102A>C
NR_027654.2:n.2108-102A>C